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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46624생성일: 2026년 10월 27일

Phenacyl bromide → alpha-(3,4-Methylenedioxyphenoxy)acetophenone

https://huagongshe.com/reaction/46624

반응식

참여 물질

역할이름HCID투입량
반응물Phenacyl bromideHCID 6259—
반응물Sodium CarbonateHCID 10340—
반응물Potassium CarbonateHCID 11430—
반응물SesamolHCID 68289—
용매BenzeneHCID 241—
생성물alpha-(3,4-Methylenedioxyphenoxy)acetophenoneHCID 20386603—

반응 단계

A mixture of 25 g. (0.181 mole) of 3,4-methylenedioxyphenol, 36 g. (0.181 mole) of α-bromoacetophenone and 41.2 g. (0.40 mole) of sodium carbonate in 350 ml. of benzene is heated to its reflux temperature and maintained at reflux for 16 hours. To the mixture is added 50 g. of potassium carbonate, and the mixture is refluxed for an additional 7 days while collecting water in a Barrett water trap. The mixture is then diluted with a mixture of water and benzene. The benzene layer is washed with water, then cold 5 percent sodium hydroxide solution. A precipitate forms in the benzene layer. It is collected, rinsed with benzene and dried to provide a white powder which is recrystallized from ethanol to provide α-(3,4-methylenedioxyphenoxy)acetophenone, m.p. 123°-126° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04174403
출처 데이터셋uspto-grants-1979_11
ORD IDord-b0a8a49ae46944b3a2df9093aa91678e
출처 메모uspto-grants-1979_11