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Sodium Hydroxide → 3-(4-Tert-butylbenzenesulfonamido)thiophene-2-carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Methyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylate | HCID 8015643 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-(4-Tert-butylbenzenesulfonamido)thiophene-2-carboxylic acid | HCID 44610603 | — |
反応手順
To a solution of 55 (0.817 g; 2.31 mmol) in methanol (4.5 mL) was added aqueous sodium hydroxide (9.2 mL; 1N). After the reaction was complete, the mixture was partitioned between diethyl ether and water; the organic layer was separated and set aside. The aqueous layer was acidified with excess aqueous hydrochloric acid (2N) and extracted with ethyl acetate (2×). The diethyl ether and ethyl acetate organic layers were combined, dried over sodium sulfate, decanted, and concentrated under reduced pressure. The resulting residue yielded the desired product a white solid from a mixture of hexanes and dichloromethane (0.54 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08178699B2 |
| 出典データセット | uspto-grants-2012_05 |
| ORD ID | ord-a7fc01462c944078a78037d3c50f0125 |
| 出典メモ | uspto-grants-2012_05 |