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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941232Generated: November 2, 2026

Methyl Morpholinoacetate → HCID 57282510, compound

https://huagongshe.com/reaction/1941232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl MorpholinoacetateHCID 1268178—
Reactant2',3'-DihydroxyacetophenoneHCID 6429110—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57282510HCID 5728251068.7%

Reaction Steps

2',3'-Dihydroxy-acetophenone (7.5 g, 49 mmole) is dissolved in 303 ml dry tetrahydrofuran in a flame dried 1,000 ml three neck round bottom flask under nitrogen. The solution is treated rapidly dropwise with potassium t-butoxide (1.0 M/THF) (197 ml, 197 mmole) and is mechanically stirred vigorously as methyl-2-(4-morpholinyl)-acetate (10.2 g, 64 mmole) is added neat. The reaction mixture is heated at reflux for 48 h, is treated with a second lot of methyl-2-(4-morpholinyl)-acetate (7 g, 44 mmole), and is stirred an additional 24h at reflux. The reaction is cooled to room temperature, is diluted with 200 ml water, and the tetrahydrofuran is removed in vacuo. The pH of the aqueous residue is adjusted to 6.8 with 10% hydrochloric acid and the mixture is extracted with 5×100 ml dichloromethane. The combined organics are dried over magnesium sulfate and are concentrated in vacuo to a brown solid. The solid is washed with 200 ml diethyl ether and is dried to afford 8.8 g of a tan solid. The solid is recrystallized twice from ethyl acetate to provide 7.5 g (60%) of the title compound as an off-white solid, mp. 202.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703075
Source datasetuspto-grants-1997_12
ORD IDord-751c36c8cdcf4e97ac2cdc9f99feb76f
Source noteuspto-grants-1997_12