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HRID 650504作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/650504

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2-(3-Chlorophenyl)-3,5,5-trimethyl-2-morpholinolHCID 9837966—

反応手順

(+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-tiimethyl-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US06274579B1
出典データセットuspto-grants-2001_08
ORD IDord-197ab059c1614a3483c1c1cc48389d32
出典メモuspto-grants-2001_08