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Hydrochloric Acid → (4S)-2,8-Dimethyl-4-[(toluenesulfonyl)amino]-5-nonanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | (2S)-4-methyl-2-(4-methylbenzenesulfonamido)pentanoic acid | HCID 768170 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 反応物 | HCID 178418529 | HCID 178418529 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | (4S)-2,8-Dimethyl-4-[(toluenesulfonyl)amino]-5-nonanone | HCID 70040285 | 41% |
反応手順
To a stirred -78° C. solution of Ts-Leu (15 g, 53 mmol) in dry THF (240 ml) was added n-butyl lithium (57.8 ml of a 0.91M solution in hexane) followed 15 minutes later by isopentyl magnesium bromide (185 ml of a 0.8M solution in THF). The mixture was heated at reflux for 3 days, then cooled and poured into 0° C. 1M HCl (500 ml). The layers were separated and the aqueous phase was extracted with ether (3×150 ml). The combined organic layers were washed with saturated NaHCO3 (2×150 ml) and brine (150 ml). Drying and evaporating provided a residue which was chromatographed on silica gel to give 7.43 g (41%) of the desired product. Mass spectrum: (M+H)+ =340.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04725583 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-8c1f3451869a4ee29ada0d2769e0ba54 |
| 出典メモ | uspto-grants-1988_02 |