Реакция #347797
ord-78e6d1cf38c14d24b7bae736936f3e0d
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Другоеdid not rise about 5° C
- 2Промывкаwashed with water
- 3СушкаThe organic layer was dried over anhydrous sodium sulfate
- 4Фильтрацияfiltered
- 5Другоеevaporated
- 6Другоеto give an oily residue
- 7ДругоеCrystallization 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.