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HRID 2417877생성일: 2026년 10월 26일

tert-Butyl acetate → 2-Bromo-3',4'-bis(pivaloyloxy)acetophenone

https://huagongshe.com/reaction/2417877

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl acetateHCID 10908—
반응물BromineHCID 24408—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물3',4'-Bis(pivaloyloxy)acetophenoneHCID 12876186—
용매ChloroformHCID 6212—
생성물2-Bromo-3',4'-bis(pivaloyloxy)acetophenoneHCID 12876187—

반응 단계

A solution of bromine (3.15 ml., 0.061 mole) in chloroform (50 ml.) was added dropwise at room temperature to a stirred solution of 3',4'-bis(pivaloyloxy)acetophenone (19.5 g., 0.016 mole) and t-butyl acetate (8.2 ml., 0.06 mole) in chloroform (150 ml.) containing a catalytic amount of anhydrous aluminium chloride (0.2 g.). The reaction mixture was stirred at room temperature for 1 hour after the addition was complete, chromatographic silica gel (75 g.) was then added and the mixture evaporated in vacuo. The residual solid was added to the top of a column of dry chromatographic silica-gel (1 kg., previously deactivated by addition of 10% w/w water and then equilibrated with 10% v/w of a 5% v/v solution of ethyl acetate in toluene). The column was developed by elution with a 5% v/v solution (1.1 l.) of ethyl acetate in toluene. The column was then eluted with ethyl acetate (2×500 ml.) and the fractions collected were monitored by thin layer chromatography (TLC) (on silica plates developed in a 50% v/v mixture of ethyl acetate and toluene). The later fractions were combined and evaporated to give 2-bromo-3',4'-bis(pivaloyloxy)acetophenone as an oil (14.2 g.) which rapidly crystallised to give a solid of m.p. 64°-66° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04470997
출처 데이터셋uspto-grants-1984_09
ORD IDord-c5e87c92a446463b9c5904c7ee9c4898
출처 메모uspto-grants-1984_09