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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1903481생성일: 2026년 10월 26일

Hydrochloric Acid → 2-Acetyl-6,7-dichloro-5-methoxybenzo[b]thiophene

https://huagongshe.com/reaction/1903481

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Acetic AnhydrideHCID 7918—
반응물6,7-Dichloro-5-methoxybenzo[b]thiopheneHCID 13289996—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2-Acetyl-6,7-dichloro-5-methoxybenzo[b]thiopheneHCID 13952874—

반응 단계

To a solution of 5.0 g of 6,7-dichloro-5-methoxybenzo[b]thiophene in 30 ml of dry tetrahydrofuran and 10 ml dry ethyl ether under nitrogen at -20° is added 11.7 ml of 2.2 M n-butyllithium, while the temperature is maintained at -20°. After stirring for 2 hours at this temperature, the reaction mixture is added dropwise through a transfer needle to a stirred solution of 22 ml of freshly distilled acetic anhydride in 40 ml of dry tetrahydrofuran at -20°. Five minutes after the addition, the reaction mixture is poured onto 100 ml 10% hydrochloric acid. The mixture is extracted twice with dichloromethane, the organic layers are collected and dried and the solvent is removed to give a solid. The solid is washed with ethyl ether to give 1.5 g of 2-acetyl-6,7-dichloro-5-methoxybenzo[b]thiophene as a fluffy solid. Recrystallization of the residue obtained by evaporation of the filtrate from ethyl ether-hexane gives an additional 0.6 g of 2-acetyl-6,7-dichloro-5-methoxybenzo[b]thiophene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04436748
출처 데이터셋uspto-grants-1984_03
ORD IDord-2236e53ed1814f6298ed5836c5cc0576
출처 메모uspto-grants-1984_03