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Phenoxyacetic Acid → 2-[N-n-propyl,N-2-(phenyloxy)ethylamino]-5-methoxytetralin
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phenoxyacetic Acid | HCID 19188 | — |
| 反応物 | Borane,N-dimethylmethanamine (1:1) | HCID 6327651 | — |
| 反応物 | 2-Propylamino-5-methoxytetralin | HCID 10242548 | — |
| 生成物 | 2-[N-n-propyl,N-2-(phenyloxy)ethylamino]-5-methoxytetralin | HCID 15228850 | — |
反応手順
A mixture of (-)-2-(N-n-propylamino)-5-methoxytetralin (80 mg, 31.9 mmol; prepared according to J. Chem. Soc., 1965, pp 26-36), phenoxyacetic acid (166 mg, 109.4 mmol) and borane trimethylamine complex (80 mg, 109.4 mmol) was refluxed in xylenes overnight. The cooled reaction mixture was extracted with NaHCO3 and the organic layer was dried over MgSo4, filtered and concentrated. The resulting oil was subjected to flash chromatography (Silica: 9:1 pet ether/EtOAc) and product was isolated with characteristic peaks at: NMR (300 MHz, CDCl3); δ 7.3-6.6 (m, 8H), 4.0(t,2H), 3.7(S,3H), 3.1-2.5(m,9H), 2.1(m,1H), 1.7-1.4(m,3H) 0.9(t,3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05274003 |
| 出典データセット | uspto-grants-1993_12 |
| ORD ID | ord-d00fd4a5353845a58ddd8c8f0af6d863 |
| 出典メモ | uspto-grants-1993_12 |