CAS: 1501-05-9; 5-Oxo-5-Phenylpentanoic Acid

该化合物是一种多用途有机化合物,其特征是苯替代氯酮和一个碳酸性功能组.其结构使它成为有机合成中有价值的中间体,特别是用于制备药品,农用化学品和特殊化学品. 氯酮和碳酸酯组为进一步衍生提供了反应性场所,有利于在凝聚反应,酯化和氨化形成中应用.其定义明确的分子框架确保了持续回流,使其适合需要精确化学转化的研究和工业过程. 该化合物在标准条件下的稳定性有利于处理和储存,而其纯度对于合成工作流程的可复制结果至关重要.

结构式图片

相似化合物

1501-04-8 833-85-2 4144-62-1

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号825-54-7 1-苯基环戊烯 | CAS号53715-97-2 5,5'-氧双(5-氧代戊酸) | CAS号23253-31-8 1-phenylcyclope... | CAS号108-55-4 戌二酸酐 | CAS号71-43-2 苯 | CAS号80706-60-1 1-oxaspiro[2.2]... | CAS号72157-46-1 2-Phenyl-cyclop... | CAS号80706-73-6 2-benzoylcyclob... | CAS号1198-34-1 Cyclopentanone,... | CAS号1011-61-6 1,5-Pentanediol... | CAS号939-52-6 4-氯-1-羰基-1-苯基丁烷 | CAS号20371-41-9 5-Phenylpentano... | CAS号826-73-3 1-苯并环庚酮 | CAS号20795-53-3 3-苯基环己酮 | CAS号2270-20-4 5-苯基戊酸 | CAS号73172-56-2 ETHYL 5-OXO-5-P... | CAS号16015-12-6 2-phenyl-3,4-di... | CAS号3350-92-3 5-phenylpent-4-... | CAS号17851-47-7 4-(2-phenyl-1,3...

合成工艺路线路线简述

    Dl-扁桃酸甲酯置于sodium Hydroxide,(Nme4)*2H2O*ch3Cn (L = Ortho-Phenylenebis(N'-Methyloxamidate)),氧气,特戊醛,Lithium Diisopropyl Amide体系中,用 乙腈 用作溶剂,化学反应 3.0H,反应生成4-苯甲酰基丁酸
    参考文献:Catalytic Aerobic Oxidative Decarboxylation Of α-Hydroxy-Acids. Methyl Mandelate As A Benzoyl Anion Equivalent
    标题:Catalytic Aerobic Oxidative Decarboxylation Of α-Hydroxy-Acids. Methyl Mandelate As A Benzoyl Anion Equivalent
    摘要:The Monomeric Square-Planar Cobalt(III) Complex Of Bis-N,N'-Disubstituted Oxamides Catalyses The Oxidative Decarboxylation Of Alpha-Hydroxy Acids With Molecular Oxygen/pivalaldehyde With Very Good Yields. This Reaction Offers An Interesting Alternative In The Use Of Methyl Mandelate As A Convenient Benzoyl Anion Equivalent. (C) 1998 Elsevier Science Ltd. All Rights Reserved.
    Doi:10.1016/s0040-4039(98)00482-1

    海关参考信息

    专利信息


    专利号:US-2022356182-A1
    优先权日:2009-03-27
    标题 :Inhibitors of hepatitis c virus replication
    发明人:COBURN CRAIG A; LUDMERER STEVEN W; LIU KUN; WU HAO; SOLL RICHARD; ZHONG BIN; ZHU JIAN
    权利人:MERCK SHARP & DOHME
    摘要:The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

    专利号:US-2005250961-A1
    优先权日:2002-06-05
    标题:Process for the preparation of 4-(4-fluorobenzoyl) butyric acid
    发明人:PULLA REDDY M
    权利人:PULLA REDDY M
    摘要:The present invention provides an improved process for the preparation of 4-(4-Fluorobenzoyl)butyric acid of formula (I), which is prepared on a commercial scale using normal quality fluorobenzene (benzene content 300-700 ppm) with the desfluoro analogue impurity at an acceptable level (less than 0.1% by HPLC). The 4-(4-Fluorobenzoyl)butyric acid has the formula (I) is a key raw material for the synthesis of anti-hyperlipoproteinemetic drug ezetimibe.

    专利号:US-11053243-B2
    优先权日:2009-03-27
    标 题:Inhibitors of hepatitis C virus replication
    发明人:COBURN CRAIG A; LUDMERER STEVEN W; LIU KUN; WU HAO; SOIL RICHARD; ZHONG BIN; ZHU JIAN
    权利人:MERCK SHARP & DOHME
    摘要:The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

    专利号:WO-03104180-A1
    优先权日:2002-06-05
    标题 :Process for the preparation of 4-(4-fluorobenzoyl) butyric acid
    发明人:PULLA REDDY MUDDASANI
    权利人:NATCO PHARMA LTD; VENKAIAH CHOWDARY NANNAPANENI; PULLA REDDY MUDDASANI
    摘要:The present invention provides an improved process for the preparation of 4-(4-Fluorobenzoyl)butyric acid of formula (I), which is prepared on a commercial scale using normal quality fluorobenzene (benzene content 300-700ppm) with the desfluoro analogue impurity at an acceptable level (less than 0.1 % by HPLC). The 4-(4-fluorobenzoyl)butyric acid has the formula (I) is a key raw material for the synthesis of anti-hyperlipoproteinemetic drug ezetimibe.

    专利号:US-9090661-B2
    优先权日:2009-03-27
    标 题:Inhibitors of hepatitis C virus replication
    发明人:COBURN CRAIG A; MCCAULEY JOHN A; LUDMERER STEVEN W; LIU KUN; VACCA JOSEPH P; WU HAO; HU BIN; SOLL RICHARD; SUN FEI; WANG XINGHAI; YAN MAN; ZHANG CHENGREN; ZHENG MINGWEI; ZHONG BIN; ZHU JIAN
    权利人:MERCK SHARP & DOHME
    摘要:The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

    专利号:US-6531470-B1
    优先权日:1998-01-23
    标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
    发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
    权利人:UPJOHN CO
    摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.
    宁波市海曙铭浩医药化工有限公司
    ⚠️ 未注册 · 未认证企业
    ⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
    数据来源于公开网络搜索,平台未作核实,请自行辨别。
    🏢敬请 企业认领
    🏬开设公司展台
    📢获取免费会员权益
    🎖️点亮专属注册企业标签
    📇展现公司完整信息 样本查看立即注册认领 →
    网址: http://www.mhpharm.com.cn
    企业联系电话:0574-88285925👤
    📞宁波市海曙铭浩医药化工有限公司 ⚠️参考联系方式
    联系人:盛先生 蔡小姐
    电话:0574-88285925
    手机:18657682767;13396618955
    传真:0574-88425889
    邮箱:sales@mhpharm.com.cn
    通信地址: 宁波市海曙区横街镇金泉路3号
    邮编: 317000
    🆔 联系时候可告知是从"百琢研"平台获取的信息.
    ⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

    地址:宁波市海曙区横街镇金泉路3号
    ⚠️ 未注册 · 未认证企业
    注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
    ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
    上海蓝润化学有限公司
    ⚠️ 未注册 · 未认证企业
    ⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
    数据来源于公开网络搜索,平台未作核实,请自行辨别。
    🏢敬请 企业认领
    🏬开设公司展台
    📢获取免费会员权益
    🎖️点亮专属注册企业标签
    📇展现公司完整信息 样本查看立即注册认领 →
    网址: http://www.longrunchem.com
    企业联系电话:021-69515658;13701998368👤
    📞上海蓝润化学有限公司 ⚠️参考联系方式
    联系人:路小姐
    电话:021-69515658;13701998368
    手机:13701998368
    传真:QQ:819185261
    邮箱:longrunchem@163.com
    通信地址: 上海市青浦区重固镇赵重公路2278号5号楼4层C区34座
    邮编: 201800
    🆔 联系时候可告知是从"百琢研"平台获取的信息.
    ⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

    地址:上海市青浦区重固镇赵重公路2278号5号楼4层C区34座
    ⚠️ 未注册 · 未认证企业
    注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
    ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
    上海康拓化工有限公司
    ⚠️ 未注册 · 未认证企业
    ⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
    数据来源于公开网络搜索,平台未作核实,请自行辨别。
    🏢敬请 企业认领
    🏬开设公司展台
    📢获取免费会员权益
    🎖️点亮专属注册企业标签
    📇展现公司完整信息 样本查看立即注册认领 →
    网址: http://www.kangtuochem.com
    企业联系电话:021-69185552;69185553;13701777608👤
    📞上海康拓化工有限公司 ⚠️参考联系方式
    联系人:陈小姐
    电话:021-69185552;69185553;13701777608
    手机:13701777608
    传真:QQ:63651968
    邮箱:kangtuochem@163.com
    通信地址: 上海市嘉定区 沙河路
    邮编: 200000
    🆔 联系时候可告知是从"百琢研"平台获取的信息.
    ⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

    地址:上海市嘉定区 沙河路
    ⚠️ 未注册 · 未认证企业
    注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
    ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
    第 1 / 1 页
    现货

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:A Facile Direct Route To N ‐(Un)Substituted Lactams By Cycloamination Of Oxocarboxylic Acids Without External Hydrogen
    作者:Hu Li,Hongguo Wu,Heng Zhang,Yaqiong Su,Song Yang,Emiel J. M. Hensen |发布日期:2019.8.22
    摘要:Lactams Are Privileged In Bioactive Natural Products And Pharmaceutical Agents And Widely Featured In Functional Materials. This Study Presents A Novel Versatile Approach To The Direct Synthesis Of Lactams From Oxocarboxylic Acids Without Catalyst Or External Hydrogen. The Method Involves The In Situ Release Of Formic Acid From Formamides Induced By Water To Facilitate Efficient Cycloamination. Water

    合成参考文献


    摘要:Zhdankin, V. V., Science of Synthesis Knowledge Updates, (2015) 1, 277.
    摘要:Vil’, V. A.; Bityukov, O. V.; Terent’ev, A. O., Science of Synthesis Knowledge Updates, (2019) 3, 406.
    摘要:Uyanik, M.; Ishihara, K., Science of Synthesis: Catalytic Oxidation in Organic Synthesis, (2017) 1, 650.
    摘要:Uyanik, M.; Ishihara, K., Science of Synthesis: Catalytic Oxidation in Organic Synthesis, (2017) 1, 654.
    摘要:Parmeggiani, F.; Galman, J. L.; Montgomery, S. L.; Turner, N. J., Science of Synthesis, (2019) , 385.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知