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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2352465생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/2352465

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 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 번호US04877440
출처 데이터셋uspto-grants-1989_10
ORD IDord-d882ecc5046840d9b1721b86a40edac0
출처 메모uspto-grants-1989_10