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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656096Generated: October 27, 2026

Tetrahydrofuran → morpholine 5-(2-Benzyloxyphenyl)-3-oxo-pent-4-ynamide

https://huagongshe.com/reaction/1656096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-AcetylmorpholineHCID 15543—
ReactantLithium diisopropylamideHCID 2724682—
ReactantMethyl-2-benzyloxyphenyl propiolateHCID 54058410—
SolventWaterHCID 962—
Productmorpholine 5-(2-Benzyloxyphenyl)-3-oxo-pent-4-ynamideHCID 8674728661%

Reaction Conditions

Temperature0 °C

Reaction Steps

Acetyl morpholine (546 ul, 4.72 mmole) was dissolved in 10 ml dry tetrahydrofuran in an oven dried 50 ml two neck round bottom flask under nitrogen. The solution was cooled to 0° C. and was treated slowly dropwise with lithium diisopropylamide (3.2 ml, 4.72 mmole). The mixture was stirred 30 minutes at 0° C. and was treated with methyl-2-benzyloxyphenyl propiolate (600 mg, 2.25 mmole) in 2 ml dry tetrahydrofuran. The reaction mixture was stirred for 1 hour at 0° C. and was diluted with 10 ml water. The volatiles were removed in vacuo and the residue was crystallized from diethyl ether/methanol (20:1). The tan solid was collected, was washed with diethyl ether, and was dried to afford 500 mg (61%) of morpholine-5-(2-Benzyloxyphenyl)-3-oxo-pent-4-ynamide as a tan solid. Melting Point: 224°-227° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252735
Source datasetuspto-grants-1993_10
ORD IDord-c4388469e9584938a636f53fdfa3d980
Source noteuspto-grants-1993_10