反应 #2383787

ord-6529ee5d522d482bb354817a8784bd4b

反应方程式

[Na]
Sodium
CCOC(=O)CS
ethyl mercaptoacetate
C=CCOC(=O)CCCCl
allyl 4-chlorobutyrate
C=CCOC(=O)CCCSCC(=O)OCC
title compound
收率 88.1%
C=CCOC(=O)CCCSCC(=O)OCC
Allyl 4-(ethoxycarbonylmethylthio)butyrate
收率 88.1%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONThe obtained solution was treated
  2. 2
    温度for 1 hour at reflux temperature
  3. 3
    浓缩The mixture was concentrated by evaporation
  4. 4
    workup.ADDITIONpoured into a mixture of diethylether (200 ml) and of an ice/water mixture (100 g)
  5. 5
    其他The ether phase was separated
  6. 6
    萃取the obtained aqueous phase was extracted with diethyl ether (200 ml)
  7. 7
    洗涤The combined ether fractions were washed with water (200 ml) and 4% aqueous sodium hydrogencarbonate solution (200 ml)
  8. 8
    干燥dried with magnesium sulfate
  9. 9
    其他After the removal of the drying agent and evaporation of ether

实验过程

Sodium (9.06 g; 0.39 mole) was decomposed in allyl alcohol (380 ml). The obtained solution was treated by dropwise adding of first ethyl mercaptoacetate (42.7 ml; 0.39 mole) at the temperature of 0° C. and then of allyl 4-chlorobutyrate (58.3 g; 0.36 mole) prepared according to the process disclosed in Example 2a. The obtained mixture was stirred for three hours at room temperature and then for 1 hour at reflux temperature. The mixture was concentrated by evaporation and poured into a mixture of diethylether (200 ml) and of an ice/water mixture (100 g). The obtained solution was acidified with 1M hydrochloric acid solution to achieve a pH value of the medium between 3 and 6. The ether phase was separated and the obtained aqueous phase was extracted with diethyl ether (200 ml). The combined ether fractions were washed with water (200 ml) and 4% aqueous sodium hydrogencarbonate solution (200 ml) and dried with magnesium sulfate. After the removal of the drying agent and evaporation of ether, the title compound (78.1 g; 84%) was obtained, which was used in the crude form in the next reaction.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06489318B1uspto-grants-2002_12