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HRID 276266作成日:2026年10月26日

Thionyl Chloride → N-(1S)-(1-(chloromethyl)-3-methylbutyl)-N-(isobutyl)amine HCl salt

https://huagongshe.com/reaction/276266

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物(2S)-4-methyl-2-(isobutylamino)pentanolHCID 22951222—
溶媒TolueneHCID 1140—
生成物N-(1S)-(1-(chloromethyl)-3-methylbutyl)-N-(isobutyl)amine HCl saltHCID 86590167—

反応条件

温度90 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06353006B1
出典データセットuspto-grants-2002_03
ORD IDord-2980885bd695465ba5c6cc0ec5da0e5d
出典メモuspto-grants-2002_03