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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1143생성일: 2026년 10월 23일

Dimethylformamide → 7-(1-Adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene

https://huagongshe.com/ko/reaction/1143

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물3-(Adamantan-1-yl)-6-bromonaphthalen-2-olHCID 14549072—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
생성물7-(1-Adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthaleneHCID 19694681—

반응 단계

11.9 g (33.3 mmol) of 7-(1-adamantyl)-6-hydroxy-2-bromonaphthalene, 120 ml of DMF, 5.1 ml (36.6 mmol) of triethylamine and 203 mg of 4-dimethylaminopyridine were introduced successively into a three-necked flask. A solution of 5.52 g (36.6 mmol) of tert-butyldimethylsilyl chloride was added dropwise and the mixture was stirred at room temperature for 12 hours. The reaction medium was poured into water, extracted with ethyl ether, the organic phase decanted, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a silica column eluted with heptane; 12 g (76%) of 7-(1-adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene of melting point 120°-121° C. were recovered.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723499
출처 데이터셋uspto-grants-1998_03
ORD IDord-a18ffbdb8f6b474a86827045ded0ce46
출처 메모uspto-grants-1998_03