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HRID 47288생성일: 2026년 10월 24일

Hydrogen Sulfide → 2-[2-(5-Bromo-2-methoxy-phenyl)-ethyl]-3-chloro-dithiobenzoic acid ethyl ester

https://huagongshe.com/ko/reaction/47288

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen SulfideHCID 402—
반응물Ether hydrochlorideHCID 10953452—
반응물2-[2-(5-Bromo-2-methoxy-phenyl)-ethyl]-3-chloro-thiobenzimidic acid ethyl esterHCID 20628395—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-[2-(5-Bromo-2-methoxy-phenyl)-ethyl]-3-chloro-dithiobenzoic acid ethyl esterHCID 20628394—

반응 조건

온도45 °C

반응 단계

As shown in Scheme 11, hydrogen sulfide gas (˜2 mL) was condensed into a cooled (−78° C.) solution of 2.8 grams (6.8 mmol) of 2-[2-(5-Bromo-2-methoxy-phenyl)-ethyl]-3-chloro-thiobenzimidic acid ethyl ester and 13.6 mL (13.6 mmol) of 1.0 M HCl/ether in 100 mL of tetrahydrofuran. The reaction was heated to 45° C. and stirred overnight in a sealed tube. The reaction mixture was diluted with water and extracted with methylene chloride once. The organic layer was washed with brine, dried (MgSO4), filtered and evaporated to give a crude orange oil. The oil was partially purified by chromatography through a short column of silica gel (eluting with 5:95 ethyl acetate/hexanes) which resulted in 1.8 g of an orange powder which was used directly in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699873B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-3d91358cdd8a44388a63432ff509d171
출처 메모uspto-grants-2004_03