Thionyl Chloride → N-(1S)-(1-(chloromethyl)-3-methylbutyl)-N-(isobutyl)amine HCl salt
反応式
[CH3:1][CH:2]([CH3:12])[CH2:3][C@H:4]([NH:7][CH2:8][CH:9]([CH3:11])[CH3:10])[CH2:5]O.O=S(Cl)[Cl:15]>C1(C)C=CC=CC=1>[ClH:15].[Cl:15][CH2:5][C@@H:4]([NH:7][CH2:8][CH:9]([CH3:11])[CH3:10])[CH2:3][CH:2]([CH3:12])[CH3:1]参加物
4
反応条件
- 温度
- 90 °C
実験手順
To a solution of (2S)-4-methyl-2-(isobutylamino)pentan-1-ol (Method B4c; 256 g, 1.5 mol) and toluene (2.5 L) was added SOCl2 (167 mL) over 15 min. After the addition of SOCl2 was complete the reaction was heated at 90° C. overnight. The reaction solution was then cooled to room temp. and concentrated under reduced pressure. The dark oily residue was dissolved in CH2Cl2 (2 L) and concentrated under reduced pressure. The red-brown residue was dissolved in Et2O (1 L), and hexane (750 mL) was added dropwise over a period of 8 h. The resulting slurry was stirred overnight, filtered, and washed with a 40% EtOAc/hex solution to give N-(1S)-(1-(chloromethyl)-3-methylbutyl)-N-(isobutyl)amine HCl salt as a dark brown solid (276 g): 1H NMR (CDCl3) δ0.93-1.00 (m, 6H), 1.10-1.12 (m, 6H), 1.85 (m, 4H), 2.24-2.34 (m, 2H), 2.80-2.88 (m, 1H), 2.90-3.02 (m, 1H), 3.50-3.57 (m, 1H), 3.96 (dd, J=12.9, 5.6 Hz, 1H), 4.10 (dd, J=13.2, 3.6 Hz, 1H).