Hydrochloric Acid → HCID 54447559, 화합물

A mixture of the above oxime (6.5 g, 31 mmol), 1,2-dibromoethane (27 ml, 31 mmol), N,N,N,N-tetrabutylammonium bromide (0.96 g, 3 mmol) and 12N sodium hydroxide (30 ml) was cooled on an icebath with vigorous stirring until the initial exotherm had subsided. The mixture was then stirred at ambient temperature for 16 h. Water (50 ml), 4 N hydrochloric acid (50 ml) and dichloromethane (100 ml) were added and the phases were separated. To the organic phase was added water (50 ml) and pH in the aqueous phase adjusted to 5 with 10% aqueous citric acid. The organic phase was washed with water (50 ml), brine (25 ml) and dried (Na2SO4). The solvent was evaporated in vacuo to give 9.1 g of 5-methoxy-1-phenyl-1-pentanone O-(2-bromoethyl)oxime.

1. temperaturewas cooled on an icebath
2. stirringThe mixture was then stirred at ambient temperature for 16 h
3. customthe phases were separated
4. additionTo the organic phase was added water (50 ml)
5. washThe organic phase was washed with water (50 ml), brine (25 ml)
6. dry with materialdried (Na2SO4)
7. customThe solvent was evaporated in vacuo

ORD 기록

ord-3066d992e0304c888db3e40a576c7fa9

출처 데이터셋

uspto-grants-1997_03

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05608069