- 英文名称2,3,5,6-Tetrafluoro-1,4-Benzenedimethanol
- 中文名称2,3,5,6-四氟对苯二甲醇
- IUPAC名称(perfluoro-1,4-phenylene)dimethanol
- 其它别名2,3,5,6-四氟-1,4-对苯二甲醇; Tetrafluoro-4-[(Hydroxymethyl)Phenyl]Methanol
- CAS编号92339-07-6
- MFCD编号:MFCD00229147
- EINECS号:814-676-7
- 分子式:C8H6F4O2
- 分子量:210.13
- 产品CID: 1961226
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
欧盟法规
C&L通报上下游产品
CAS号652-36-8 四氟对苯二甲酸 | CAS号727-55-9 2,3,5,6-四氟对苯二甲酸二甲酯 | CAS号950-70-9 2,3,5,6-tetrafl... | CAS号963-46-2 diethyl 2,3,5,6... | CAS号3217-47-8 2,3,5,6-四氟对二苯甲醛 | CAS号123-91-1 1,4-二氧六环 | CAS号7440-02-0 镍 | CAS号95-50-1 邻二氯苯 | CAS号719-32-4 2,3,5,6-四氯对苯二甲酰氯 | CAS号79538-03-7 2,3,5,6-四氟-4-甲基苯甲醇 | CAS号703-87-7 四氟-对-二甲苯 | CAS号83282-91-1 四氟对甲氧基甲基苯甲醇 | CAS号131803-37-7 2,3,5,6-四氟-1,4-... | CAS号776-40-9 2,3,5,6-四氟对二溴苄合成工艺路线路线简述
- 15041-74-4 = 92339-07-6
反应条件:1.1 Reagents: Tetrabutylammonium Chloride,Zinc Chloride,Sodium Borohydride Solvents: Tetrahydrofuran; Rt1.2 Solvents: Tetrahydrofuran; Rt -> Reflux; 8 H,Reflux
标题:Synthesis Of 4-Methyl-2,3,5,6-Tetrafluorobenzyl Alcohol
作者:Yuan,Qi-Liang; Qian,Jie; Shi,Zheng-Jun; Bao,Zhang-Feng; Zeng,Jun
参考文献:Huaxue Shijie 日期:2014 卷标:55(5) 页码:285-288]
15041-74-4 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Catalysts: Tetrabutylammonium Chloride,Aluminum Chloride Solvents: Tetrahydrofuran; Rt; Rt -> Reflux; 8 H,Reflux; Reflux -> Rt1.2 Reagents: Hydrochloric Acid Solvents: Water
标题:Research On Synthesis Of 2,3,5,6-Tetrafluoro-4-Methoxyl Methyl Benzyl Alcohol
作者:Yuan,Qiliang; Shi,Zhengjun; Qian,Jie; Zhang,Jiabing; Chen,Haifeng
参考文献:Huagong Shengchan Yu Jishu 日期:2013 卷标:20(6) 页码:11-14]
727-55-9 = 92339-07-6
反应条件:1.1 Reagents: Calcium Chloride Solvents: Ethanol,Water; 30 Min,15 °C1.2 Reagents: Potassium Tetrafluoroborate; 2 H,15 °C
标题:Method For Preparation Of Tetrafluoro-P-Phenylenedimethanol With Reduced Waste Discharge Using Calcium Chloride
参考文献:China]
652-36-8 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: 1,2-Dimethoxyethane; 1 H,50 °C; 7 H,60 °C1.2 Solvents: Toluene; 60 °C -> 50 °C1.3 Reagents: Hydrochloric Acid Solvents: Water; 1 H,50 °C; 6 H,60 °C
标题:Process For Preparation Of 4-Methyl-2,3,5,6-Tetrafluorobenzyl Alcohol
参考文献:World Intellectual Property Organization]
652-36-8 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: 1,2-Dimethoxyethane; Rt -> 50 °C; 1 H,50 °C; 7 H,60 °C1.2 Solvents: Ethanol; 60 °C -> 50 °C1.3 Reagents: Hydrochloric Acid Solvents: Water; 6 H,60 °C
标题:Method For Producing Halogen-Substituted Benzenedimethanols
参考文献:World Intellectual Property Organization]
727-55-9 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: Tetrahydrofuran; Rt1.2 Reagents: Hydrochloric Acid Solvents: Tetrahydrofuran,Water; 5 H,Rt; 2 H,25 - 30 °C
标题:Process For Production Of Halogen-Substituted Benzenedimethanol
参考文献:World Intellectual Property Organization]
727-55-9 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: Tetrahydrofuran; 30 Min,Reflux; 3 H,Reflux; 7 H,Reflux1.2 Reagents: Sulfuric Acid Solvents: Water; Neutralized
标题:Synthesis Of "Black Hole" 4,4'-Bipyridinium Cyclophane
作者:Xi,Hai-Tao; Sun,Xiao-Qiang; Wei,Hai-Lin; Meng,Qi; Pan,Yi; Et Al
参考文献:Youji Huaxue 日期:2007 卷标:27(12) 页码:1547-1551]
652-36-8 = 92339-07-6
反应条件:1.1 Reagents: Sodium Hydride Solvents: Tetrahydrofuran; Rt -> 65 °C1.2 Solvents: Water; 3 H,65 °C; 2 H,65 °C1.3 Reagents: Hydrochloric Acid Solvents: Water; 30 Min,25 - 30 °C
标题:Method For Producing Halogen-Substituted Benzenedimethanol
参考文献:World Intellectual Property Organization]
727-55-9 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: Ethanol; 5 H,50 °C1.2 Reagents: Hydrochloric Acid Solvents: Water
标题:Preparation Of 2,3,5,6-Tetrafluoro-1,4-Benzenedimethanol As Intermediate For Pyrethroids
参考文献:World Intellectual Property Organization]
652-36-8 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: Methanol; 5 H,50 °C
标题:Novel Process For The Preparation Of [2,3,5,6-Tetrafluoro-4-(Methoxymethyl)Phenyl]Methyl 2,2,3,3-Tetramethylcyclopropanecarboxylate
参考文献:China]
15041-74-4 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: Tetrahydrofuran; 6 H,85 °C1.2 Reagents: Hydrochloric Acid Solvents: Water
标题:Preparation Of 2,3,5,6-Tetrafluoro-1,4-Benzenedimethanol From 2,3,5,6-Tetrafluoro-1,4-Benzenedicarbonyl Dichloride
参考文献:China]
15041-74-4 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: Chlorobenzene; 0.5 H,70 °C1.2 Catalysts: Iodine Solvents: Chlorobenzene; 0.5 H,70 °C; 7 H,70 °C; 70 °C -> 50 °C1.3 Reagents: Hydrochloric Acid Solvents: Water; 50 °C; 0.5 H,Ph 1 - 2,50 °C1.4 Reagents: Sodium Hydroxide Solvents: Water; Ph 8 - 9
标题:A Process For Preparing 2,3,5,6-Tetrafluoro-1,4-Benzenedimethanol
参考文献:China]
7154-26-9 = 92339-07-6
反应条件:1.1 Reagents: Hydrofluoric Acid Solvents: Dimethylformamide; 7 H,120 °C
标题:Preparation Of 2,3,5,6-Tetrafluoro-Terephthalic Alcohol
参考文献:China]
652-36-8 = 92339-07-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: 1,2-Dimethoxyethane1.2 Reagents: Dimethyl Sulfate Solvents: Toluene
标题:Process For The Preparation Of Halogen-Substituted Dibenzyl Alcohols By The One-Step Reduction Of The Corresponding Halogen-Substituted Terephthalic Acids Using Sodium Boranates And Alkylation Agents
参考文献:European Patent Organization]
89992-50-7 = 92339-07-6
反应条件:1.1 Solvents: Acetic Acid,Water1.2 Reagents: Sodium Nitrite Solvents: Water1.3 Reagents: Sodium Hydroxide Solvents: Water
标题:Preparation Of 4-Methyl-2,3,5,6-Tetrafluorobenzyl Alcohol
参考文献:World Intellectual Property Organization]
327-54-8 = 92339-07-6
反应条件:1.1 Reagents: Sulfuric Acid,Chlorosulfonic Acid Catalysts: Zinc Chloride; 3 H,45 °C; 2 H,58 °C1.2 Reagents: Sodium Carbonate Solvents: Ethanol,Water; 10 H,Reflux
标题:Process For Preparation Of 2,3,5,6-Tetrafluoro-1,4-Benzenedimethanol
参考文献:China]
89992-50-7 = 92339-07-6
反应条件:1.1 Reagents: Sodium Nitrite Solvents: Water; 30 Min,Rt; Rt -> 0 °C1.2 Reagents: Acetic Acid; 1 H,40 °C1.3 Reagents: Sodium Bicarbonate Solvents: Water; 1 H,40 °C
标题:Method For The Preparation Of Benzene-Dimethanol
参考文献:Japan]
89992-50-7 = 92339-07-6
反应条件:1.1 Reagents: Sodium Nitrite Solvents: Water1.2 Reagents: Acetic Acid1.3 Reagents: Sodium Bicarbonate
标题:Production Method For Benzenedimethanol Compound
参考文献:World Intellectual Property Organization]
727-55-9 = 92339-07-6
反应条件:1.1 Reagents: Potassium Borohydride Solvents: 1,2-Dimethoxyethane; 20 - 25 °C; 25 °C -> Reflux; 2 H,Reflux; Cooled1.2 Reagents: Sulfuric Acid Solvents: Water; Ph 1 - 2,Cooled
标题:Synthesis Of Tetramethylfluthrin
作者:He,Shu-Ze
参考文献:Xiandai Nongyao 日期:2014 卷标:13(6) 页码:22-24]
950-71-0 = 92339-07-6
反应条件:1.1 Catalysts: 4-(Dimethylamino)Pyridine Solvents: Acetonitrile; Rt -> 80 °C1.2 Reagents: Di-Tert-Butyl Dicarbonate; 2 H,80 °C; 2 H,80 °C1.3 Reagents: Sodium Borohydride Solvents: Tetrahydrofuran; Rt -> 50 °C; 2 H,50 °C1.4 Reagents: Methanol; 1 H,50 °C; 1 H,50 °C
标题:Method For Producing Halogen-Substituted Benzenedimethanol
参考文献:World Intellectual Property Organization
四氟对苯二腈置于盐酸,Copper(II) Chromite,水,氢气体系中,用 甲醇,甲基叔丁基醚 作为反应溶剂,-10.0~65.0 °C,9.8 Mpa 条件下,反应 10.0H,反应生成 2,3,5,6-四氟对苯二甲醇
参考文献:一种制备2,3,5,6-四氟-1,4-对苯二甲醇的工艺
标题:一种制备2,3,5,6-四氟-1,4-对苯二甲醇的工艺
摘要:本发明公开了一种制备2,3,5,6‑四氟‑1,4‑对苯二甲醇的工艺,属于精细化学品合成技术领域,包括以下反应步骤:(1)2,3,5,6‑四氟‑1,4‑对苯二甲腈在醚类溶剂中,通入干燥的氯化氢气体进行反应,然后加入低碳醇进行反应,得2,3,5,6‑四氟‑1,4‑对苯二甲酸亚氨基酯的溶液;(2)2,3,5,6‑四氟‑1,4‑对苯二甲酸亚氨基酯与水反应,收集有机相,水洗至中性,真空蒸馏脱除溶剂,得2,3,5,6‑四氟‑1,4‑对苯二甲酸二酯;(3)2,3,5,6‑四氟‑1,4‑对苯二甲酸二酯进行催化加氢还原反应,收集有机相,冷却,抽滤,烘干,得2,3,5,6‑四氟‑1,4‑对苯二甲醇.本发明具有原料廉价,操作简便,不产生高浓度酸性废水等优点.
专利信息
专利号:US-10745334-B2
优先权日:2018-12-21
标题 :Method for synthesizing 2,3,5,6-tetrafluoro-4-methoxymethyl benzyl alcohol
发明人:YUAN QILIANG; ZHANG JINGDE; CHEN HAIFENG; CUI YIXIN; CHEN YINHAO; WANG CHAO
权利人:ZHEJIANG ZHONGXIN FLUORIDE MAT CO LTD
摘要:The disclosure discloses a method for synthesizing 2,3,5,6-tetrafluoro-4-methoxymethyl benzyl alcohol from 1,4-bis(methoxymethyl)-2,3,5,6-tetrafluorobenzene, belongings to the technical field of organic synthesis. 1,4-bis(methoxymethyl)-2,3,5,6-tetrafluorobenzene reacts in mixed solution consisting of sulfuric acid aqueous solution and organic carboxylic acid, the obtained mixture is subjected to ester group hydrolysis reaction in the presence of an inorganic base and then to hydroxyl methylation reaction, 2,3,5,6-tetrafluoro-4-methoxymethyl benzyl alcohol is finally obtained via separation and purification, and 1,4-bis(methoxymethyl)-2,3,5,6-tetrafluorobenzene is recovered. The disclosure not only realizes the resource utilization of low-value 1,4-bis(methoxymethyl)-2,3,5,6-tetrafluorobenzene, and meanwhile has the advantages of mild reaction conditions, simple operation, high synthesis yield, good product quality and the like. The disclosure has high social and economic values.
专利号:CN-219784763-U
优先权日:2023-05-30
标 题 :A kind of transfluthrin intermediate synthesis device