Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl 3-(aminosulfonyl)-2-thiophenecarboxylate → 2-(Hydroxymethyl)thiophene-3-sulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl 3-(aminosulfonyl)-2-thiophenecarboxylate | HCID 101012 | — |
| 반응물 | Lithium borohydride | HCID 4148881 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(Hydroxymethyl)thiophene-3-sulfonamide | HCID 14254937 | 41.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04743290 |
| 출처 데이터셋 | uspto-grants-1988_05 |
| ORD ID | ord-c05cdcf7574e4c4cb07a343f8ed48be9 |
| 출처 메모 | uspto-grants-1988_05 |