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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33754생성일: 2026년 10월 23일

Oxalyl chloride → 6-Methoxy-1-benzothiophene-2,3-dione

https://huagongshe.com/ko/reaction/33754

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물3-MethoxybenzenethiolHCID 84989—
반응물Aluminum(III) ChlorideHCID 6451240—
용매Diethyl EtherHCID 3283—
생성물6-Methoxy-1-benzothiophene-2,3-dioneHCID 344084847.4%

반응 단계

To a solution of 3-methoxythiophenol (3.75 g, 26.7 mmol) in ether (20 mL) was added oxalyl chloride (3.7 mL, 43 mmol) dropwise. The mixture was heated at reflux for 1.5 h, cooled to rt, and concentrated in vacuo. The resulting yellow oil was dissolved in dichloromethane (50 mL), cooled to 0° C., and was treated with aluminum chloride (4.30 g, 32.0 mmol) in portions. The mixture was heated at reflux for 30 min, cooled to rt, and poured onto ice water with stirring. The organic layer was separated and successively washed with saturated, aqueous sodum bicarbonate, water, and brine. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography (4/1 ethyl acetate/hexane) which provided 2.46 g (47%) of 6-methoxy-1-benzothiophene-2,3-dione as an orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429664B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-7b4b5dc5d57c4724a2802c423685f17d
출처 메모uspto-grants-2008_09