戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 890587作成日:2026年10月26日

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

https://huagongshe.com/reaction/890587

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US06998400B2
出典データセットuspto-grants-2006_02
ORD IDord-e43afa0563794aef96bd00890f1acd8f
出典メモuspto-grants-2006_02