Реакция #2195491

ord-7b127bc3693746dfa1966eeb2ca6dda8

Уравнение реакции

Cc1ccc(S)cc1
4-methylbenzenethiol
[H-].[Na+]
NaH
CCOC(=O)CBr
Ethylbromoacetate
CCOC(=O)CSc1ccc(C)cc1
colorless oil
Выход 99.0%
CCOC(=O)CSc1ccc(C)cc1
p-Tolylsulfanyl-acetic acid ethyl ester
Выход 99.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGfurther stirred at room temperature for 3 h
  2. 2
    ДругоеThe solvent was removed under vacuum
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in dil. HCl
  4. 4
    Экстракцияextracted by ethylacetate
  5. 5
    ПромывкаThe combined organic phase was washed successively with saturated NaHCO3 solution, water and brine
  6. 6
    Сушкаthen dried over Na2SO4
  7. 7
    ДругоеEvaporation of organic phase

Методика

A solution of 4-methylbenzenethiol (5 g, 40.25) in dry THF was added dropwise to a suspension of NaH (60% in mineral oil, 1.98 g, 48.30) in THF at room temperature and stirred for 30 min. under N2 atmosphere. Ethylbromoacetate (4.9 mL, 44.27) was added slowly to this solution and further stirred at room temperature for 3 h. The solvent was removed under vacuum. The residue was dissolved in dil. HCl and extracted by ethylacetate. The combined organic phase was washed successively with saturated NaHCO3 solution, water and brine then dried over Na2SO4. Evaporation of organic phase yielded 8.46 g (99%) colorless oil. 1H NMR (CDCl3): δ 1.22 (t, J=7.2 Hz, 3H), 2.32 (s, 3H), 3.57 (s, 2H), 4.14 (q, J=7.2 Hz, 2H), 7.11 (d, J=8.0 Hz, 2H), 7.33 (d, J=8.0 Hz, 2H). EIMS m/z 210 (M+1), 233 (M+23).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07514225B2uspto-grants-2009_04