Реакция #347797

ord-78e6d1cf38c14d24b7bae736936f3e0d

Уравнение реакции

Cc1ccc2ccccc2c1O
2-methyl-1-naphthol
CCN(CC)CC
triethylamine
CC(=O)Cl
acetyl chloride
CC(=O)Oc1c(C)ccc2ccccc12
title compound
Выход 63.1%
CC(=O)Oc1c(C)ccc2ccccc12
1-acetoxy-2-methylnaphthalene
Выход 63.1%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеdid not rise about 5° C
  2. 2
    Промывкаwashed with water
  3. 3
    СушкаThe organic layer was dried over anhydrous sodium sulfate
  4. 4
    Фильтрацияfiltered
  5. 5
    Другоеevaporated
  6. 6
    Другоеto give an oily residue
  7. 7
    ДругоеCrystallization in hexane

Методика

A solution of 9.48 g (60 mmole) of 2-methyl-1-naphthol and 8.10 g (80 mmole) of triethylamine in 50 mL of ethyl acetate was cooled to below 5° C. in an ice-bath. 5.50 g (70 mmole) of acetyl chloride was added at a rate such that the temperature did not rise about 5° C. The reaction mixture was stirred for an additional one hour, diluted with 50 mL of ethyl acetate, and washed with water then brine. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to give an oily residue. Crystallization in hexane yielded 7.58 g (63% yield) of the title compound with a melting point of 81°-83° C. and an 1HNMR as follows: (300 MHz, DMSO-d6) δ 2.26 ) (s, 3H), 2.48 (s, 3H), 7.42 (d, 1H, J=9 Hz), 7.46-7.55 (m, 2H), 7.47-7.81 (m, 2H), 7.92 (d, 1H, J=9 Hz). The mass spectrum showed a molecular ion at m/z 200.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05529583uspto-grants-1996_06