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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1252352생성일: 2026년 10월 23일

Methyl 3-(aminosulfonyl)-2-thiophenecarboxylate → 2-(Hydroxymethyl)thiophene-3-sulfonamide

https://huagongshe.com/ko/reaction/1252352

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-(aminosulfonyl)-2-thiophenecarboxylateHCID 101012—
반응물Lithium borohydrideHCID 4148881—
용매TetrahydrofuranHCID 8028—
생성물2-(Hydroxymethyl)thiophene-3-sulfonamideHCID 1425493741.2%

반응 단계

To 5.0 g of methyl 3-aminosulfonylthiophene-2-carboxylate in 200 mL of tetrahydrofuran was added 0.75 g of lithium borohydride. After heating at reflux for two hours the reaction was quenched with water and acidified with concentrated hydrochloric acid. The desired product was then extracted into methylene chloride which was washed with water, dried over magnesium sulfate, filtered and concentrated in vacuo to yield 1.8 g of a yellow solid, m.p. 85°-89°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04743290
출처 데이터셋uspto-grants-1988_05
ORD IDord-c05cdcf7574e4c4cb07a343f8ed48be9
출처 메모uspto-grants-1988_05