摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-乙酰氧基-2-(乙酰氧基甲基)-2-甲基丙酸 | 17872-58-1

中文名称
3-乙酰氧基-2-(乙酰氧基甲基)-2-甲基丙酸
中文别名
——
英文名称
2,2-bis(acetoxymethyl)propionic acid
英文别名
3-acetyloxy-2-(acetyloxymethyl)-2-methylpropanoic acid
3-乙酰氧基-2-(乙酰氧基甲基)-2-甲基丙酸化学式
CAS
17872-58-1
化学式
C9H14O6
mdl
——
分子量
218.207
InChiKey
OQZAEPCZSVMOSK-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.1
  • 重原子数:
    15
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    89.9
  • 氢给体数:
    1
  • 氢受体数:
    6

安全信息

  • 海关编码:
    2918990090

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-乙酰氧基-2-(乙酰氧基甲基)-2-甲基丙酸 在 palladium on activated charcoal 4-二甲氨基吡啶草酰氯氢气三乙胺N,N-二甲基甲酰胺 作用下, 以 二氯甲烷乙酸乙酯 为溶剂, 反应 2.0h, 生成 3-(3-Acetoxy-2-acetoxymethyl-2-methyl-propionyloxy)-2-(3-acetoxy-2-acetoxymethyl-2-methyl-propionyloxymethyl)-2-methyl-propionic acid
    参考文献:
    名称:
    Synthesis, Characterization, and 1H NMR Self-Diffusion Studies of Dendritic Aliphatic Polyesters Based on 2,2-Bis(hydroxymethyl)propionic Acid and 1,1,1-Tris(hydroxyphenyl)ethane
    摘要:
    Dendritic aliphatic polyesters of one, two, three, and four generations (M(w): 906, 1856, 3754, and 7549 g/mol) were synthesized in the convergent fashion, using 2,2-bis(hydroxymethyl)propionic acid as building block and 1,1,1-tris(hydroxyphenyl)ethane as core molecule. Dendrons of one to four generations were synthesized from the building block and in a final step coupled to the core molecule. The focal point of the dendrons was protected by a benzyl ester group and deprotected by catalytic hydrogenolysis. The esterifications were performed by conversion of the acid into the corresponding acid chloride and followed by reaction of the acid chloride with the hydroxyl groups in the presence of triethylamine and dimethylaminopyridine. The simplicity of the H-1-NMR and C-13-NMR spectras and elemental analyses suggest that pure and monodisperse dendrimers were obtained. Molecular selfdiffusion studies of first, second, third, and fourth generation dendrimers were performed, in chloroform, using pulsed-field spin echo H-1 NMR spectroscopy. The self-diffusion coefficients were calculated with the standard form of the Stejskal-Tanner equation. The effective radii of the dendrimers were estimated from the diffusion coefficients by assuming a spherical geometry for all dendrimers. The radii obtained were 7.8, 10.3, 12.6, and 17.1 Angstrom for the first, second, third, and fourth generation dendrimer, respectively.
    DOI:
    10.1021/ja954171t
  • 作为产物:
    描述:
    2,2-二羟甲基丙酸乙酰氯4-二甲氨基吡啶三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 0.5h, 以98%的产率得到3-乙酰氧基-2-(乙酰氧基甲基)-2-甲基丙酸
    参考文献:
    名称:
    Synthesis, Characterization, and 1H NMR Self-Diffusion Studies of Dendritic Aliphatic Polyesters Based on 2,2-Bis(hydroxymethyl)propionic Acid and 1,1,1-Tris(hydroxyphenyl)ethane
    摘要:
    Dendritic aliphatic polyesters of one, two, three, and four generations (M(w): 906, 1856, 3754, and 7549 g/mol) were synthesized in the convergent fashion, using 2,2-bis(hydroxymethyl)propionic acid as building block and 1,1,1-tris(hydroxyphenyl)ethane as core molecule. Dendrons of one to four generations were synthesized from the building block and in a final step coupled to the core molecule. The focal point of the dendrons was protected by a benzyl ester group and deprotected by catalytic hydrogenolysis. The esterifications were performed by conversion of the acid into the corresponding acid chloride and followed by reaction of the acid chloride with the hydroxyl groups in the presence of triethylamine and dimethylaminopyridine. The simplicity of the H-1-NMR and C-13-NMR spectras and elemental analyses suggest that pure and monodisperse dendrimers were obtained. Molecular selfdiffusion studies of first, second, third, and fourth generation dendrimers were performed, in chloroform, using pulsed-field spin echo H-1 NMR spectroscopy. The self-diffusion coefficients were calculated with the standard form of the Stejskal-Tanner equation. The effective radii of the dendrimers were estimated from the diffusion coefficients by assuming a spherical geometry for all dendrimers. The radii obtained were 7.8, 10.3, 12.6, and 17.1 Angstrom for the first, second, third, and fourth generation dendrimer, respectively.
    DOI:
    10.1021/ja954171t
点击查看最新优质反应信息

文献信息

  • NOVEL NITROSO COMPOUNDS AS NITROXYL DONORS AND METHODS OF USE THEREOF
    申请人:Frost Lisa M.
    公开号:US20090281062A1
    公开(公告)日:2009-11-12
    The invention relates to nitroso derivatives including carboxylic acid and phosphoric acid esters of hydroxy nitroso compounds that donate nitroxyl (HNO) under physiological conditions. The compounds and compositions of the invention are useful in treating and/or preventing the onset and/or development of diseases or conditions that are responsive to nitroxyl therapy, including heart failure, ischemia/reperfusion injury and cancer.
    本发明涉及亚硝基衍生物,包括在生理条件下捐赠亚硝基(HNO)的羟基亚硝基化合物的羧酸和磷酸酯。发明中的化合物和组合物可用于治疗和/或预防对亚硝基疗法有响应的疾病或病症的发作和/或发展,包括心力衰竭、缺血/再灌注损伤和癌症。
  • Silver-Catalyzed Decarboxylative Bromination of Aliphatic Carboxylic Acids
    作者:Xinqiang Tan、Tao Song、Zhentao Wang、He Chen、Lei Cui、Chaozhong Li
    DOI:10.1021/acs.orglett.7b00439
    日期:2017.4.7
    The silver-catalyzed Hunsdiecker bromination of aliphatic carboxylic acids is described. With Ag(Phen)2OTf as the catalyst and dibromoisocyanuric acid as the brominating agent, various aliphatic carboxylic acids underwent decarboxylative bromination to provide the corresponding alkyl bromides under mild conditions. This method not only is efficient and general but also enjoys wide functional group
    描述了银催化的脂肪族羧酸的Hunsdiecker溴化。以Ag(Phen)2 OTf为催化剂,二溴异氰尿酸为溴化剂,各种脂肪族羧酸经过脱羧溴化,在温和条件下提供相应的烷基溴化物。该方法不仅高效通用,而且具有广泛的功能组兼容性。提出了涉及Ag(II)中间体的氧化自由基机理。
  • Silver-Catalyzed Decarboxylative Fluorination of Aliphatic Carboxylic Acids in Aqueous Solution
    作者:Feng Yin、Zhentao Wang、Zhaodong Li、Chaozhong Li
    DOI:10.1021/ja3048255
    日期:2012.6.27
    industries, general and site-specific C(sp(3))-F bond formations are still a challenging task. We report here that with the catalysis of AgNO(3), various aliphatic carboxylic acids undergo efficient decarboxylative fluorination with SELECTFLUOR(®) reagent in aqueous solution, leading to the synthesis of the corresponding alkyl fluorides in satisfactory yields under mild conditions. This radical fluorination
    尽管氟化化合物已在化学和材料行业中得到广泛应用,但一般和特定于站点的 C(sp(3))-F 键的形成仍然是一项具有挑战性的任务。我们在此报告,在 AgNO(3) 的催化作用下,各种脂肪族羧酸在水溶液中使用 SELECTFLUOR(®) 试剂进行有效的脱羧氟化,从而在温和条件下以令人满意的产率合成相应的烷基氟化物。这种自由基氟化方法不仅高效通用,而且具有化学选择性和官能团相容性,因此在氟化分子的合成中具有很高的实用性。对于这种催化氟脱羧,提出了一种涉及 Ag(III) 介导的单电子转移,然后是氟原子转移的机制。
  • A General Approach to Quaternary Center Construction from Couplings of Unactivated Alkenes and Acyl Xanthates
    作者:Ernest N. Jenkins、William L. Czaplyski、Erik J. Alexanian
    DOI:10.1021/acs.orglett.7b00882
    日期:2017.5.5
    to quaternary center construction using unactivated alkenes as coupling partners is reported. In this strategy, acyl xanthates, readily accessed from carboxylic acids, serve as precursors to tertiary radicals. This strategy leverages the unique reactivity of xanthates to participate in efficient radical-mediated additions to unactivated alkenes, expanding the scope of quaternary center construction
    据报道,使用未活化的烯烃作为偶合伙伴的,由自由基介导的四元中心构建的一般方法。在这种策略中,容易从羧酸中获得的酰基黄药作为叔自由基的前体。该策略利用了黄药的独特反应性,以有效地将自由基介导的加成物加到未活化的烯烃中,从而扩大了季铵盐中心的建设范围。
  • Silver-Catalyzed Decarboxylative Allylation of Aliphatic Carboxylic Acids in Aqueous Solution
    作者:Lei Cui、He Chen、Chao Liu、Chaozhong Li
    DOI:10.1021/acs.orglett.6b00802
    日期:2016.5.6
    Direct decarboxylative radical allylation of aliphatic carboxylic acids is described. With K2S2O8 as the oxidant and AgNO3 as the catalyst, the reactions of aliphatic carboxylic acids with allyl sulfones in aqueous CH3CN solution gave the corresponding alkenes in satisfactory yields under mild conditions. This site-specific allylation method is applicable to all primary, secondary, and tertiary alkyl
    描述了脂肪族羧酸的直接脱羧自由基烯丙基化。以K 2 S 2 O 8为氧化剂,AgNO 3为催化剂,脂肪族羧酸与烯丙基砜在CH 3 CN水溶液中的反应在温和条件下以令人满意的收率得到了相应的烯烃。此位点特定的烯丙基化方法适用于所有伯,仲和叔烷基酸,并具有广泛的官能团相容性。
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物