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Isobutyraldehyde → (4S)-4-Isobutyl-2-isopropyloxazolidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isobutyraldehyde | HCID 6561 | — |
| 反応物 | L-Leucinol | HCID 111307 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (4S)-4-Isobutyl-2-isopropyloxazolidine | HCID 45096513 | 100.2% |
反応手順
A solution of (1S)-1-(hydroxymethyl)-3-methylbutylamine (Method B1b; 152 g, 1.3 mol) and isobutyraldehyde (118 mL, 1.3 mol, 1.0 equiv.) in toluene (1.5 L) was heated at the reflux temp. until the theoretical amount of water had been collected in a Dean-Stark trap (23.4 mL). The reaction mixture was concentrated by distillation to approximately 700 mL. The resulting mixture was cooled to room temp. and was concentrated under reduced pressure to a constant weight to give (4S)-2-isopropyl-4-isobutyl-1,3-oxazolidine as a pale yellow oil (223 g, 100%): 1H NMR (CDCl3) δ0.88-0.99 (m, 12H), 1.18-1.35 (m, 1H), 1.42-1.56 (m, 1H), 1.61-1.79 (m, 4H), 3.08 (t, J=7.4 Hz 1H), 3.20-3.34 (m, 1H), 3.85 (t, J=7.4 Hz, 1H), 4.18 (dd, J=7.3, 3.4 Hz, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06353006B1 |
| 出典データセット | uspto-grants-2002_03 |
| ORD ID | ord-71ca128157574f968e5f7a17729a53c5 |
| 出典メモ | uspto-grants-2002_03 |