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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24572생성일: 2026년 10월 23일

Ethanethiol → 2-Bromo-5,6-dihydro-5,5-dimethyl8-(ethylthio)-naphthalene

https://huagongshe.com/ko/reaction/24572

반응식

참여 물질

역할이름HCID투입량
반응물EthanethiolHCID 6343—
반응물TriethylamineHCID 8471—
반응물7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10753357—
촉매Titanium TetrachlorideHCID 24193—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-Bromo-5,6-dihydro-5,5-dimethyl8-(ethylthio)-naphthaleneHCID 22571521—

반응 단계

To a solution of 1.03 g (4.1 mmol) of 7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one (Compound G) in 30.0 mL of tetrahydrofuran, was added dropwise 0.49 g (0.85 mL, 7.8 mmol) of titaniumtetrachloride and the resulting solution stirred for 10 min. A solution of 35 mg (0.50 mL, 6.7 mmol) of ethanethiol and 0.54 g (0.75 mL, 5.4 mmol) of triethylamine in 10.0 mL of tetrahydrofuran was added and the reaction stirred at room temperature for 13 h. The mixture was diluted with water and extracted with ether (2×). The organic phase was washed with brine, dried over Na2SO4 and then concentrated in vacuo. Purification by flash chromatography (silica, 100% hexane) gave the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855832B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-57924e275c8e4ebe90a25748051ba105
출처 메모uspto-grants-2005_02