Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976503Generated: October 28, 2026

Dimethyl Sulfoxide → HCID 53913346, compound

https://huagongshe.com/reaction/976503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantStyrene OxideHCID 7276—
Reactant(4-Benzylmorpholin-2-yl)methanolHCID 2776358—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
ProductHCID 53913346HCID 5391334629.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4.30 g of 4-benzyl-2-hydroxymethylmorpholine, 930 mg of potassium tert-butoxide and 4 ml of dimethyl sulfoxide was heated to 80° C. Thereto was dropwise added 2.50 g of styrene oxide over 20 minutes. The resulting mixture was stirred for 2 hours at the same temperature. The reaction mixture was added to a mixture of 30 ml of diethyl ether and 30 ml of ice water. The organic layer was separated and mixed with 10 ml of water. The mixture was adjusted to pH 2.0 with 6N hydrochloric acid. The aqueous layer was separated and mixed with 30 ml of diethyl ether. The mixture was adjusted to pH 11 with a 2N aqueous sodium hydroxide solution. The organic layer was separated, washed with a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography (eluant: toluene/ethyl acetate=1/1) to obtain 2.00 g of oily 1-phenyl-2-[(4-benzylmorpholin-2-yl)methoxy]ethanol (compound No. 144).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612381
Source datasetuspto-grants-1997_03
ORD IDord-4f087289056e4b88b1c7932ccc47bbb4
Source noteuspto-grants-1997_03