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HRID 2352465作成日:2026年10月27日

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

https://huagongshe.com/reaction/2352465

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-(aminosulfonyl)-2-thiophenecarboxylateHCID 101012—
反応物Lithium borohydrideHCID 4148881—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Hydroxymethyl)thiophene-3-sulfonamideHCID 1425493741.2%

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04877440
出典データセットuspto-grants-1989_10
ORD IDord-d882ecc5046840d9b1721b86a40edac0
出典メモuspto-grants-1989_10