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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650504Generated: October 26, 2026

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

https://huagongshe.com/reaction/650504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
ReactantBupropion Morpholinol (2R,3R)-IsomerHCID 9943907—
SolventWaterHCID 962—
Product2-(3-Chlorophenyl)-3,5,5-trimethyl-2-morpholinolHCID 9837966—

Reaction Steps

(+/−)-(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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274579B1
Source datasetuspto-grants-2001_08
ORD IDord-197ab059c1614a3483c1c1cc48389d32
Source noteuspto-grants-2001_08