Реакция #2383786

ord-94d63f3bf0544516b297b5d11806b7ff

Уравнение реакции

O=C(O)CCCCl
4-chlorobutyric acid
C=CCO
allyl alcohol
CCCCCC
hexane
C=CCOC(=O)CCCCl
title compound
Выход 79.0%
C=CCOC(=O)CCCCl
Allyl 4-chlorobutyrate
Выход 79.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added
  2. 2
    ТемператураThe obtained mixture was heated for 5 hours
  3. 3
    Другоеwas simultaneously removed with Dean-Stark apparatus (Vogel's Textbook of Practical Organic Chemistry, Fourth Ed., Longman, London, 1978, p. 411)
  4. 4
    СушкаThe obtained solution was dried with magnesium sulfate
  5. 5
    Фильтрацияafter the filtration of the drying agent hexane
  6. 6
    Другоеwas evaporated
  7. 7
    workup.DISTILLATIONThe crude residue was distilled under reduced pressure 10 mbar at the temperature of 95° C.

Методика

To a mixture of 4-chlorobutyric acid (48 ml; 0.48 mole), allyl alcohol (200 ml) and hexane (1.2 l) p-toluenesulfonic acid (16.0 g; 0.08 mole) was added. The obtained mixture was heated for 5 hours at reflux temperature in such a way that water was simultaneously removed with Dean-Stark apparatus (Vogel's Textbook of Practical Organic Chemistry, Fourth Ed., Longman, London, 1978, p. 411). The mixture was then cooled to room temperature and shaken with 7% aqueous sodium hydrogencarbonate solution (2×500 ml). The obtained solution was dried with magnesium sulfate and after the filtration of the drying agent hexane was evaporated. The crude residue was distilled under reduced pressure 10 mbar at the temperature of 95° C. and the title compound (61.2 g; 79%) was obtained in the form of a colourless oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06489318B1uspto-grants-2002_12