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HRID 496708생성일: 2026년 10월 23일

tert-Butyl bromoacetate → tert-Butyl 4-(2,6-difluorophenyl)-4-oxobutyrate

https://huagongshe.com/ko/reaction/496708

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl bromoacetateHCID 79177—
반응물1-(2,6-Difluorophenyl)ethan-1-oneHCID 83643—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물tert-Butyl 4-(2,6-difluorophenyl)-4-oxobutyrateHCID 21964547—

반응 조건

온도-60 °C

반응 단계

To a stirred solution of 2,6-Difluoroacetophenone (5 g, 32 mmol) in dry THF (40 ml) and DMPU (8 ml) was added a solution of lithium bis(trimethylsilyl)amide (1.0M, 45 ml) at 60° C. under argon. After stirring for 10 minutes at −60° C., tert-Butyl bromoacetate (6.99 g, 35.8 mmol) was added rapidly. The reaction mixture was stirred for an additional 10 minutes and then warmed to room temperature for 4 hours. The crude mixture was taken in EtOAc and washed with water and brine. The aqueous layer was extracted one more time with EtOAc. The combined organic layers were dried over Na2SO4, filtered, concentrated and purified by flash chromatography on a silica gel column (hex:ethyl acetate, 2:1) to provide the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06946491B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-75c5547bbc3e4b39aeea5bb4d92c18bf
출처 메모uspto-grants-2005_09