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-(2-methyl-5-oxotetrahydrofuran-2-yl) 4-oxopentanoic acid | 856219-95-9

中文名称
——
中文别名
——
英文名称
3-(2-methyl-5-oxotetrahydrofuran-2-yl) 4-oxopentanoic acid
英文别名
3-(2-Methyl-5-oxooxolan-2-yl)-4-oxopentanoic acid
3-(2-methyl-5-oxotetrahydrofuran-2-yl) 4-oxopentanoic acid化学式
CAS
856219-95-9
化学式
C10H14O5
mdl
——
分子量
214.218
InChiKey
UYNYFEJBGNEWRD-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

物化性质

  • 沸点:
    431.0±15.0 °C(Predicted)
  • 密度:
    1.248±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.4
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    80.7
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] PROCESS FOR HYDROGENATION<br/>[FR] PROCÉDÉ POUR L'HYDROGÉNATION
    申请人:SHELL INT RESEARCH
    公开号:WO2011015643A1
    公开(公告)日:2011-02-10
    A process for the hydrogenation of a reactant selected from: (a) a 5- or 6-membered lactone that is substituted at the ring-closing carbon atom and has a proton at a carbon atom adjacent to the ring-closing carbon atom; (b) an ester of a carboxylic acid having a gamma- carbonyl group and a proton at a carbon atom adjacent to the carbon atom of the carbonyl group; and (c) a carboxylic acid having a gamma-carbonyl group and a proton at a carbon atom adjacent to the carbon atom of the carbonyl group, which process involves contacting the reactant with a catalyst in the presence of hydrogen, at a temperature from 100 to 3500C and a pressure from 1 to 150 bar (absolute), provided the pressure is low enough to avoid condensation of the heaviest feed component at the temperature chosen, and wherein the catalyst is a weakly acidic heterogeneous catalyst comprising a hydrogenating metal.
    一种用于氢化反应物的方法,所选反应物包括:(a) 在环闭合碳原子处取代的5-或6-成员内酯,且在环闭合碳原子相邻的碳原子上有质子;(b) 具有γ-羰基和在羰基碳原子相邻的碳原子上有质子的羧酸酯;以及(c) 具有γ-羰基和在羰基碳原子相邻的碳原子上有质子的羧酸,该方法涉及将反应物与催化剂接触在氢气存在下,温度在100至350°C,压力在1至150 bar(绝对值)范围内进行,前提是压力足够低以避免在所选温度下最重的进料组分的凝结,并且催化剂是弱酸性的异质催化剂,包括氢化金属。
  • PROCESS FOR HYDROGENATION
    申请人:Lange Jean-Paul
    公开号:US20110112326A1
    公开(公告)日:2011-05-12
    A process for the hydrogenation of a reactant selected from: (a) a 5- or 6-membered lactone that is substituted at the ring-closing carbon atom and has a proton at a carbon atom adjacent to the ring-closing carbon atom; (b) an ester of a carboxylic acid having a gamma-carbonyl group and a proton at a carbon atom adjacent to the carbon atom of the carbonyl group; and (c) a carboxylic acid having a gamma-carbonyl group and a proton at a carbon atom adjacent to the carbon atom of the carbonyl group, which process involves contacting the reactant with a catalyst in the presence of hydrogen, at a temperature from 100 to 350° C. and a pressure from 1 to 150 bar (absolute), provided the pressure is low enough to avoid condensation of the heaviest feed component at the temperature chosen, and wherein the catalyst is a weakly acidic heterogeneous catalyst comprising a hydrogenating metal.
    一种用于氢化反应物的方法,所述反应物选自:(a)在环闭合碳原子处取代并在环闭合碳原子相邻碳原子处有质子的5-或6-成员内酯;(b)具有γ-羰基和在γ-羰基相邻碳原子处有质子的羧酸酯;以及(c)具有γ-羰基和在γ-羰基相邻碳原子处有质子的羧酸,该方法涉及将反应物与催化剂在氢气存在下接触,在温度为100至350°C和压力为1至150巴(绝对)的条件下,只要压力足够低以避免在所选温度下使最重的进料组分凝结,并且所述催化剂是弱酸性的异质催化剂,包括氢化金属。
  • [EN] PROCESS FOR PREPARING AN ESTER<br/>[FR] PROCÉDÉ POUR LA PRÉPARATION D'UN ESTER
    申请人:SHELL INT RESEARCH
    公开号:WO2011015385A1
    公开(公告)日:2011-02-10
    A process for preparing an ester of formula (I): R3CH2- (CR1R2)n-CH2-O-CO-(CR1R2)n-CH2R3 (I) wherein n is 1-3 and R1 and R2 are each, independently, a hydrogen atom or a carbon-linked organic group and R3 is a carbon-linked organic group, by hydrogenation of a reactant selected from: (a) a lactone of formula (II) wherein n is 1-3 and R1 and R2 are each, independently, a hydrogen atom or a carbon-linked organic group and R3 is a carbon-linked organic group; (b) an ester of a carboxylic acid of formula (III) R4-O-CO- (CR1R2)n-CO-R3 (III) wherein n is 1-3 and R1 and R2 are each, independently, a hydrogen atom or a carbon-linked organic group and R3 and R4 are a carbon-linked organic group; and c) a carboxylic acid of formula (IV) H-O-CO- (CR1R2)n-CO-R3 (IV) wherein n is 1-3 and R1 and R2 are each, independently, a hydrogen atom or a carbon-linked organic group and R3 is a carbon-linked organic group; which process involves contacting the reactant with a heterogeneous catalyst comprising a hydrogenating metal in the presence of hydrogen, wherein the catalyst is a zeolite-free heterogeneous catalyst comprising a hydrogenating metal supported on a metal oxide or a mixed oxide.
    制备式(I)酯的过程:R3CH2- (CR1R2)n-CH2-O-CO-(CR1R2)n-CH2R3 (I),其中n为1-3,R1和R2分别独立地为氢原子或碳链有机基团,R3为碳链有机基团,通过选择的反应物的加氢制备:(a)式(II)内酯,其中n为1-3,R1和R2分别独立地为氢原子或碳链有机基团,R3为碳链有机基团;(b)式(III)羧酸酯,其中n为1-3,R1和R2分别独立地为氢原子或碳链有机基团,R3和R4为碳链有机基团;和(c)式(IV)羧酸,其中n为1-3,R1和R2分别独立地为氢原子或碳链有机基团,R3为碳链有机基团;该过程涉及将反应物与含有氢化金属的非均相催化剂接触,在氢气存在下,其中催化剂是一种不含沸石的非均相催化剂,包括负载在金属氧化物或混合氧化物上的氢化金属。
  • HYDROGENATION PROCESS FOR THE CONVERSION OF A CARBOXYLIC ACID OR AN ESTER HAVING A CARBONYL GROUP
    申请人:Haan Johan Rene
    公开号:US20070208183A1
    公开(公告)日:2007-09-06
    A hydrogenation process for the conversion of a reactant selected from the group consisting of a carboxylic acid having a carbonyl group and an ester of a carboxylic acid having a carbonyl group to form a carboxylic acid or an ester with a hydroxyl group or a lactone, wherein the reactant is contacted with a heterogeneous catalyst comprising a hydrogenating compound, in the presence of formic acid, at a temperature in the range of from 150 to 400° C. and a pressure in the range of from 1.0 to 150 bar (absolute).
    一种氢化工艺,用于将来自以下组的反应物转化为具有羟基或内酯的羧酸或羧酸酯:具有羰基的羧酸或羧酸酯的酯,其中将反应物与含有氢化合物的非均相催化剂接触,在甲酸存在下,在温度为150至400℃和压力为1.0至150巴(绝对值)的范围内进行。
  • Renewable hydrocarbons, method for producing the same and use thereof
    申请人:NESTE OYJ
    公开号:US10968397B2
    公开(公告)日:2021-04-06
    A method for conversion of levulinic acid and to a hydrocarbon composition obtainable by the method. The method includes a step of providing a feedstock, a conversion step of subjecting the feedstock to a C—C coupling reaction and a hydrotreatment, and a hydrodeoxygenation step. The content of levulinic acid dimer derivatives having 4 oxygen atoms subjected to the hydrodeoxygenation step is 20 wt.-% or more.
    一种转化乙酰丙酸和可通过该方法获得的碳氢化合物组合物的方法。该方法包括提供原料步骤、将原料进行 C-C 偶联反应和加氢处理的转化步骤以及加氢脱氧步骤。经过加氢脱氧步骤的具有 4 个氧原子的乙酰丙酸二聚体衍生物的含量为 20 wt.-% 或更多。
查看更多

同类化合物

马来酰基乙酸 顺-3-己烯-1-丙酮酸 青霉酸 钠氟草酰乙酸二乙酯 醚化物 酮霉素 辛酸,2,4-二羰基-,乙基酯 草酸乙酯钠盐 草酰乙酸二乙酯钠盐 草酰乙酸二乙酯 草酰乙酸 草酰丙酸二乙酯 苯乙酰丙二酸二乙酯 苯丁酸,b-羰基-,2-丙烯基酯 聚氧化乙烯 羟基-(3-羟基-2,3-二氧代丙基)-氧代鏻 磷酸二氢2-{(E)-2-[4-(二乙胺基)-2-甲基苯基]乙烯基}-1,3,3-三甲基-3H-吲哚正离子 碘化镝 硬脂酰乙酸乙酯 甲氧基乙酸乙酯 甲氧基乙酰乙酸酯 甲基氧代琥珀酸二甲盐 甲基4-环己基-3-氧代丁酸酯 甲基4-氯-3-氧代戊酸酯 甲基4-氧代癸酸酯 甲基4-氧代月桂酸酯 甲基4-(甲氧基-甲基磷酰)-2,2,4-三甲基-3-氧代戊酸酯 甲基3-羰基-2-丙酰戊酸酯 甲基3-氧代十五烷酸酯 甲基2-氟-3-氧戊酯 甲基2-氟-3-氧代己酸酯 甲基2-氟-3-氧代丁酸酯 甲基2-乙酰基环丙烷羧酸酯 甲基2-乙酰基-4-甲基-4-戊烯酸酯 甲基2-乙酰基-2-丙-2-烯基戊-4-烯酸酯 甲基2,5-二氟-3-氧代戊酸酯 甲基2,4-二氟-3-氧代戊酸酯 甲基2,4-二氟-3-氧代丁酸酯 甲基1-异丁酰基环戊烷羧酸酯 甲基1-乙酰基环戊烷羧酸酯 甲基1-乙酰基环丙烷羧酸酯 甲基(2Z,4E,6E)-2-乙酰基-7-(二甲基氨基)-2,4,6-庚三烯酸酯 甲基(2S)-2-甲基-4-氧代戊酸酯 甲基(1R,2R)-2-乙酰基环丙烷羧酸酯 瑞舒伐他汀杂质 瑞舒伐他汀杂质 环氧乙烷基甲基乙酰乙酸酯 环戊戊烯酸,Β-氧代,乙酯 环戊基(氧代)乙酸乙酯 环戊[b]吡咯-6-腈,八氢-2-氧-,[3aS-(3aalpha,6alpha,6aalpha)]-(9CI)