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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41640생성일: 2026년 10월 23일

Methanol → Methyl 3-bromothiophene-2-carboxylate

https://huagongshe.com/ko/reaction/41640

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Thionyl ChlorideHCID 24386—
반응물3-Bromothiophene-2-carboxylic acidHCID 2739688—
생성물Methyl 3-bromothiophene-2-carboxylateHCID 2740074—

반응 단계

3-Bromothiophene-2-carboxylic acid (5.0 g, 24 mmol, 1 eq.) was dissolved in MeOH (100 mL) and the mixture was degassed and purged with nitrogen (2×). SOCl2 (15 mL, 0.2 mol, 8.3 eq.) was added dropwise and the resulting mixture was stirred overnight at room temperature. The mixture was then concentrated and DCM (150 mL) was added. Saturated NaHCO3 (20 mL) was added, and the resulting mixture was stirred at room temperature for 15 minutes. The organic layer was washed with saturated NaHCO3 (20 mL), water (20 mL), and saturated aqueous NaCl (20 mL), then dried over Na2SO4, filtered and concentrated to yield 3-bromothiophene-2-carboxylic acid methyl ester (4.0 g) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530663B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-80167fa325ac4c73b8b6b32d36edcb90
출처 메모uspto-grants-2013_09