CAS: 5464-28-8; (1,3-Dioxolan-4-yl)Methanol

该化合物是一种多用途循环烷醇,其分子式为C4H8O3.它具有二氧烷环状结构,具有氢氧甲基替代成分,在氢氧基组和丙烯功能中都可进行再活性.该化合物作为合成化学中一种受保护的甘油或甘蓝丁二烯的一种保护形式,具有特别宝贵的价值,能够在温和条件下进行选择性变异.在基本和中性条件下,其稳定性,加上其进行酸催化环开关的能力,使它成为有机合成,制药和聚合化学的有用中间体.乙醇的极性(1,3-二氧基-4-yl)也增强了普通有机溶剂的溶性,促进了其在多步骤合成溶剂中的应用.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号98238-47-2 4-(phenylmethox... | CAS号50-00-0 甲醛 | CAS号56-81-5 甘油 | CAS号109-87-5 甲缩醛 | CAS号7647-01-0 盐酸 | CAS号7664-93-9 硫酸 | CAS号110-88-3 三聚甲醛 | CAS号19921-29-0 4-(pentoxymethy... | CAS号19921-31-4 4-(hexoxymethyl... | CAS号32061-16-8 Benzenesulfonic... | CAS号126121-31-1 4-(2-methylprop... | CAS号98238-47-2 4-(phenylmethox...

合成工艺路线路线简述

    4-((Benzyloxy)Methyl)-1,3-Dioxolane置于钯 氢气体系中,用 正庚烷 作为反应溶剂,化学反应 48.0H,以75%的收率获得产物甘油缩甲醛
    参考文献:Predvoditelev; Malenkovskaya; Nifant'Ev,Russian Journal Of General Chemistry,1998,Vol. 68,# 6,P. 881-886
    标题:Predvoditelev; Malenkovskaya; Nifant'Ev,Russian Journal Of General Chemistry,1998,Vol. 68,# 6,P. 881-886

    海关参考信息

    专利信息


    专利号:US-2010099894-A1
    优先权日:2006-10-09
    标 题 :Method for the Synthesis of Cyclic Acetals by the Reactive Extraction of a Polyol in a Concentrated Solution
    发明人:DUBOIS JEAN-LUC; IBORRA CHORNET SARA; VELTY ALEXANDRA I LUCIENNE; CORMA CANOS AVELINO
    权利人:DUBOIS JEAN-LUC; IBORRA CHORNET SARA; VELTY ALEXANDRA I LUCIENNE; CORMA CANOS AVELINO
    摘要:A method for the synthesis of cyclic acetals comprises reacting at least one carbonyl-function compound selected from aldehydes, ketones, and/or linear acetals, on a polyol in a concentrated aqueous solution exceeding 20 wt % in a reactor containing an acidic catalyst. The carbonyl-function compound is selected so that the cyclic acetal obtained has a water solubility lower than 20000 mg/kg. During the catalytic reaction for the cyclic acetal synthesis, at least one portion of the organic phase containing the cyclic acetal is separated. The acidic catalysis is either homogeneous when using a water-soluble strong acid, or heterogeneous when using a solid acid such as a resin, a zeolite, or any appropriately acidified solid. The extractive reaction method can be used for obtaining high conversions and selectivity.

    专利号:WO-9900440-A1
    优先权日:1997-06-26
    标 题:Synthesis of a dendritic polyalcohol
    发明人:IHRE HENRIK; HULT ANDERS
    权利人:PERSTORP AB; IHRE HENRIK; HULT ANDERS
    摘要:A process for a double stage convergent synthesis of a polymeric polyalcohol substantially and preferably built up from polyester units and composed of a monomeric or polymeric core to which at least one hyperbranched dendritic branch (dendron) consisting of a number of branching generations is added. The branching generations comprise a polymeric or monomeric branching chain extender having three reactive functions of which two are hydroxyl groups and one is a carboxyl group. The two hydroxyl groups of the branching chain extender is in a first step ketal protected by reacting said two hydroxyl groups with a ketal. A second step includes protection of the carboxyl group of said branching chain extender. The ketal protected branching chain extender and the carboxyl protected chain extender are then employed for repeated addition in a number of step yielding a predetermined number of branching generations. The thus synthesized dendron is finally added to a core having reactive hydroxyl or epoxide groups and the ketal protected hydroxyl groups are optionally deprotected.

    专利号:US-11717498-B2
    优先权日:2013-12-31
    标题 :Methods of treatment using amphetamine controlled release, prodrug, and abuse deterrent dosage forms
    发明人:POPP KARL; MECKLER HAROLD
    权利人:Chemapotheca LLC; PHARMAPOTHECA A INC
    摘要:The invention also relates to pharmaceutical compositions comprising highly pure amphetamine and amphetamine-class compounds resulting from the synthesis of chiral and racemic amphetamine derivatives by stereospecific, regioselective cuprate addition reaction with aziridine phosphoramidate compounds, and to methods of manufacturing, delivering, and using the amphetamine compounds resulting from the synthesis of chiral and racemic amphetamine derivatives by stereospecific, regioselective cuprate addition reaction with aziridine phosphoramidate compounds.

    专利号:US-4814347-A
    优先权日:1985-07-22
    标 题:Anthelmintic spiroketals and method of use
    发明人:NELSON STEPHEN J
    权利人:UPJOHN CO
    摘要:This invention pertains to a new method for killing and controlling worms (Helminths), new formulations for killing and controlling worms in animals, new chemical compounds, and a new synthesis of northern hemisphere intermediates for the synthesis of milbemycin and avermectin macrolides.

    专利号:US-6211329-B1
    优先权日:1997-06-26
    标题:Process for preparation of a dendritic polyol
    发明人:REHNBERG NICOLA; PETTERSSON BO; ANNBY ULF; MALMBERG MATS
    权利人:PERSTORP AB
    摘要:A process for synthesis of a polymeric polyalcohol substantially and preferably built up form polyester units and composed of a monomeric or polymeric initiator molecule to which at least one dentritic branch (dendron) consisting of a number of branching generations is added. The branching generations comprise a polymericor monomeric branching chain extender having three reactive functions of which two are hydroxyl groups. The two hydroxyl groups of the ranching chain extender is acetal protected by reaction between said two hydroxyl groups and an acetal-forming carbonyl compound, preferably an aldehyde. The acetal protected branching chain extender is then employed for addition to the initiator molecule of a first branching generation followed by an optional deprotection of the hydroxyl groups by decomposition of acetals and for addition in repeated steps of further branching generations. Additions of branching generations individually employ an acetal protected branching chain extender synthesized from the same or a different branching chain extender and/or acetal-forming carbonyl compound and addition of a branching generation is optionally followed by addition of a spacing generation.

    专利号:US-6051711-A
    优先权日:1997-10-24
    标 题 :Synthesis of swainsonine salts
    发明人:TROPPER FRANCOIS; SHAH RAJAN N; SHARMA PRADEEP
    权利人:GLYCODESIGN INC
    摘要:A method for synthesizing swainsonine salts and intermediates thereof comprising subjecting a compound of the formula I wherein R2 and R2' are the same or different and represent alkyl, halogen, alkenyl, alkoxy, cycloalkyl or aryl which may be substituted, to acid hydrolysis in the presence of a C1-4 alkanol to obtain a crystalline salt of swainsonine; and optionally, recrystallizing the swainsonine salt from a C1-4 alkanol. The reaction may be used in combination with one or more additional reaction steps.
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    合成参考文献


    参考文献:10.1111/j.2042-7158.1959.tb12538.x
    摘要:SANDERSON DM. A note on glycerol formal as a solvent in toxicity testing. J Pharm Pharmacol. 1959 Mar;11(3):150–6. doi: 10.1111/j.2042-7158.1959.tb12538.x.
    摘要:S104 | UKVETMED | UK Veterinary Medicines Directorate's List | DOI:10.5281/zenodo.7802119
    摘要:REPROTOX - Scialli AR, Lione A, Boyle Padgett GK. Reproductive Effects of Chemical, Physical, and Biological Agents. Baltimore: The Johns Hopkins University Press, 1995.
    摘要:Annales Pharmaceutiques Francaises., 44(293), 1986 []
    摘要:Kouklovsky, C., Science of Synthesis, (2007) 29, 572.
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