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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 465872생성일: 2026년 10월 24일

Triethylamine → 3-[[Dimethyl(1,1,2-trimethylpropyl)silyl]oxy]benzene bromide

https://huagongshe.com/ko/reaction/465872

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-BromophenolHCID 11563—
반응물Dimethylthexylsilyl chlorideHCID 144239—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물3-[[Dimethyl(1,1,2-trimethylpropyl)silyl]oxy]benzene bromideHCID 1987540794.8%

반응 단계

To a stirred solution of 3-bromophenyl alcohol (5.0 g, 26.7 mmol) and triethylamine (3.25 g, 32.1 mmol) in anhydrous CH2Cl2 (125 mL) at room temperature under argon was added dropwise dimethylthexylsilylchloride (5.26 g, 29.4 mmol). After 1.5 hours, 4-dimethylaminopyridine (0.50 g) was added and the stirring was continued for an additional 3 hours. The reaction mixture was diluted with hexane (200 mL) and the precipitate was filtered off. The filtrate was concentrated, partitioned between hexane (200 mL) and 1N aqueous HCl (3×40 mL), and the organic layer was washed with saturated aqueous NaHCO3 (2×40 mL). The organic layer was dried (MgSO4), filtered and concentrated to yield title bromide (8.01 g, 91%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05153327
출처 데이터셋uspto-grants-1992_10
ORD IDord-2120ce38006b45ea849d9d008495a88d
출처 메모uspto-grants-1992_10