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Dichloromethane → 1-Methyl-1,2,3,4-tetrahydroquinoline-7-sulfonyl chloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | 1,2,3,4-Tetrahydro-1-methylquinoline | HCID 68109 | — |
| 反応物 | HCID 178527254 | HCID 178527254 | — |
| 生成物 | 1-Methyl-1,2,3,4-tetrahydroquinoline-7-sulfonyl chloride | HCID 53414197 | 8% |
反応手順
A solution of 1-methyl-1,2,3,4-tetrahydroquinoline (10 g, 68.03 mmol) in dichloromethane (20 mL) was added dropwise to HSO3Cl (80 g, 689.66 mmol) at 0-5° C., and the resulting solution was maintained at room temperature overnight. The reaction mixture was then quenched by adding 300 mL of iced water. The resulting solution was extracted using ethyl acetate (3×150 mL). The organic layers were combined, concentrated, and the residue was purified by column chromatography using a 1:20 ethyl acetate/petroleum ether solvent system to afford 1-methyl-1,2,3,4-tetrahydroquinoline-7-sulfonyl chloride as a yellow liquid in 8% yield. 1H NMR (CDCl3) δ 7.19 (d, 1H), 7.10 (d, 1H), 7.06 (s, 1H), 3.33 (t, 2H), 2.97 (s, 3H), 2.81 (d, 2H), 1.99 (m, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07696229B2 |
| 出典データセット | uspto-grants-2010_04 |
| ORD ID | ord-0b5a9f789336410781473493566b8633 |
| 出典メモ | uspto-grants-2010_04 |