化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → HCID 53655042、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 1-[4-(2-Hydroxy-ethoxy)-phenyl]-3-phenyl-propan-1-one | HCID 18798689 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 53655042 | HCID 53655042 | — |
反応手順
A solution of 1-[4-(2-hydroxy-ethoxy)-phenyl]-3-phenyl-propan-1-one (prepared in Example N; 6.0 g, 22.2 mmol) and triethylamine (NEt3) (4.60 mL, 33.3 mmol) in CH2Cl2 (50 mL) was cooled to 0° C. under a nitrogen atmosphere and treated with mesyl chloride (2.1 mL, 26.6 mmol). The mixture allowed to stir for 45 minutes, and then diluted with additional CH2Cl2 and washed with H2O. The organic layer was dried (MgSO4) and the solvent removed in vacuo to provide the title compound which was used without further purification. 1H NMR (DMSO-d6) δ 2.90 (t, 2 H), 3.20 (s, 3 H), 3.29 (t, 2 H), 4.32-4.34 (m, 2 H), 4.52-4.55 (m, 2 H), 7.05 (d, 2 H), 7.22-7.32 (m, 5 H), 7.95 (d, 2 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06046355 |
| 出典データセット | uspto-grants-2000_04 |
| ORD ID | ord-e8c97de80d8a4a2c874cef9d2eb4b4f9 |
| 出典メモ | uspto-grants-2000_04 |