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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59676생성일: 2026년 10월 24일

N-bromobutanimide → Methyl 2-bromomethyl-6-(tert-butyldimethylsilyloxy)benzoate

https://huagongshe.com/ko/reaction/59676

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물Methyl 2-(tert-butyldimethylsilyloxy)-6-methylbenzoateHCID 89705147—
촉매AzobisisobutyronitrileHCID 6547—
촉매TungstenHCID 23964—
용매Carbon TetrachlorideHCID 5943—
생성물Methyl 2-bromomethyl-6-(tert-butyldimethylsilyloxy)benzoateHCID 2517026132.7%

반응 단계

N-Bromosuccinimide (7.6 g) was added to a solution of methyl 2-(tert-butyldimethylsilyloxy)-6-methylbenzoate (Intermediate 13, 11.9 g) in carbon tetrachloride (150 mL) and the mixture was stirred and heated to reflux. Azo-bis-isobutyronitrile (0.1 g) was added and the mixture was illuminated with a 500 W tungsten filament lamp for 2 hours. The mixture was cooled and left to stand overnight then filtered through a 25 g silica cartridge eluting with a mixture of ethyl acetate and pentane (20%). The eluent was evaporated to dryness and the residue was redissolved in carbon tetrachloride (150 mL) and N-bromosuccinimide (6.96 g) was added. The mixture was heated to reflux and azo-bis-isobutyronitrile (0.1 g) was added. The resultant mixture was illuminated with a 500 W tungsten filament lamp overnight. After cooling, the mixture was filtered and the solid was washed with pentane. The combined organic solutions were evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of TBME and pentane with a gradient of 0-10% to give methyl 2-bromomethyl-6-(tert-butyldimethylsilyloxy)benzoate (4.99 g) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440943B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-36a2e59214c242a194b845bfaf3a9823
출처 메모uspto-grants-2016_09