乙醇 → HCID 118268374，化合物

HRID 1663014笔记

反应方程式

HRID 1663014 反应方程式
[CH:1]1([S:4][C:5]2[CH:10]=[CH:9][C:8]([CH2:11][C:12]([OH:14])=[O:13])=[CH:7][CH:6]=2)[CH2:3][CH2:2]1.S(Cl)(Cl)=O.[CH2:19](O)[CH3:20]>>[CH2:19]([O:13][C:12](=[O:14])[CH2:11][C:8]1[CH:9]=[CH:10][C:5]([S:4][CH:1]2[CH2:2][CH2:3]2)=[CH:6][CH:7]=1)[CH3:20]

参与物

4

反应物 3

HCID 702乙醇HCID 24386氯化亚砜HCID 59347115[4-(Cyclopropylsulfanyl)phenyl]acetic acid

产物 1

HCID 118268374HCID 118268374，化合物

实验过程

[4-(Cyclopropylthio)phenyl]acetic acid (13.1 g) was dissolved into ethanol (52 mL). Then, thionyl chloride (5.51 mL) was added dropwise while cooling by an ice bath, and the resulting mixture was stirred for 90 minutes at room temperature. This reaction mixture was concentrated under reduced pressure, and the resulting residue was dissolved in ethyl acetate (125 mL). This ethyl acetate solution was washed with water (4×25 mL) and then a saturated aqueous sodium carbonate solution (25 mL). The resulting mixture was dried over anhydrous sodium sulfate, then filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluant; hexane:ethyl acetate=3:1) to obtain ethyl[4-(cyclopropylthio)phenyl]acetate (15.5 g).

后处理

  1. temperaturewhile cooling by an ice bath
  2. concentrationThis reaction mixture was concentrated under reduced pressure
  3. dissolutionthe resulting residue was dissolved in ethyl acetate (125 mL)
  4. washThis ethyl acetate solution was washed with water (4×25 mL)
  5. dry with materialThe resulting mixture was dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe resulting residue was purified by silica gel column chromatography (eluant; hexane:ethyl acetate=3:1)

来源与证据

ORD记录
ord-6966b730f59a402eae078b5e54155911
来源数据集
uspto-grants-2011_10
专利号
US08034819B2

反应笔记

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