Реакция #1090306

ord-18096ab61afd4e16bd6790e4ed237d60

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 Hz, 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: US06045590uspto-grants-2000_04