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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357739생성일: 2026년 10월 23일

Methyl 3-bromothiophene-2-carboxylate → 3-Bromothiophene-2-carboxylic acid

https://huagongshe.com/ko/reaction/357739

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-bromothiophene-2-carboxylateHCID 2740074—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
용매Sodium HydroxideHCID 14798—
생성물3-Bromothiophene-2-carboxylic acidHCID 273968897.3%

반응 단계

3-Bromo-2-thiophenecarboxylic acid methyl ester (7.74 g) was dissolved in a mixture of methanol (35 ml) and tetrahydrofuran (35 ml), and 1N aqueous sodium hydroxide (53 ml) was added. The mixture was stirred at room temperature for 2 hours and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 3-bromo-2-thiophenecarboxylic acid (7.05 g) as crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840917
출처 데이터셋uspto-grants-1998_11
ORD IDord-2e768a02cf3442ff911f2d68e5377a5c
출처 메모uspto-grants-1998_11