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HRID 11209作成日:2026年10月24日

Diethyl Ether → (2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol

https://huagongshe.com/ja/reaction/11209

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Sodium HydroxideHCID 14798—
反応物Bupropion Morpholinol (2R,3R)-IsomerHCID 9943907—
溶媒WaterHCID 962—
生成物(2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinolHCID 9943908—

反応手順

(+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride may be converted back to its free base by the following process. A 3.0 g sample of (+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride was dissolved in water (100 mL) and diethyl ether was added (200 mL). The mixture was chilled in an ice bath and the pH was adjusted to >10 with 1.0N aqueous sodium hydroxide. After stirring for 30 min., the phases were separated and the aqueous phase was extracted with diethyl ether. The combined diethyl ether extracts were dried (Na2SO4) and concentrated in vacuo to give 2.6 g of (+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol as a white solid. This was used without further purification for the chiral chromatography described below.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098206B2
出典データセットuspto-grants-2006_08
ORD IDord-ccf1d5796b1247748d63c86e697ede67
出典メモuspto-grants-2006_08