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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1363487생성일: 2026년 10월 23일

Oxalyl chloride → 4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carbonyl chloride

https://huagongshe.com/ko/reaction/1363487

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물4,5,6,7-Tetrahydro-1-benzothiophene-2-carboxylic acidHCID 2063443—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carbonyl chlorideHCID 6485362—

반응 조건

온도0 °C

반응 단계

4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carboxylic acid (1.0 g, 5.50 mmol) is dissolved in dichloromethane [DCM] (25 mL) that contains 5 drops of N,N-dimethylformamide [DMF] under nitrogen and cooled to 0° C. Oxalyl chloride (13.7 mL of a 2.0M solution in DCM) is added via syringe and allowed to warm to RT over 1 hour. All solvent is then removed under reduced pressure, and the resultant oil is reduced from toluene (3×20 mL) to remove residual oxalyl chloride. The residue is then dissolved in ethyl acetate and washed with saturated sodium bicarbonate (1×100 mL), then washed with saturated sodium chloride (1×100 mL) and dried over sodium sulfate. The solution is then filtered and concentrated under reduced pressure to give 4,5,6,7-tetrahydro-benzo[b]thiophene-2-carbonyl chloride (8) as an off-white solid (1.03 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07884108B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-87845a04017d4e2bbbc86c4637470a31
출처 메모uspto-grants-2011_02