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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580604Generated: October 25, 2026

Water → 4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholide

https://huagongshe.com/reaction/580604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantPhosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl esterHCID 11207805—
Reactant4-Amino-3,4',5-trichlorobenzophenoneHCID 13373314—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholideHCID 54521919—

Reaction Steps

A solution of 5.3 g (0.02 mol) of diethylphosphonoacetic acid morpholide in 100 ml of dry tetrahydrofuran was slowly added dropwise, while stirring, to a suspension of 1 g of sodium hydride (0.02 mol, 50% in oil) in 50 ml of dry tetrahydrofuran. Slight heating and strong foaming occurred. After all had been added, the mixture was stirred for 10 minutes more. A solution of 3 g (0.01 mol) of 4-amino-3,4',5-trichlorobenzophenone in 20 ml of dry tetrahydrofuran was added dropwise to the resulting clear solution, and the mixture was heated for 16 hours at reflux temperature. After cooling, the solution was poured into water, and the aqueous mixture was extracted exhaustively with methylene chloride. The methylene chloride phase was dried with sodium sulfate and evaporated by evaporation in vacuo. The residue was crystallized from isopropanol/petroleum ether. The colorless crystals thus obtained, melting point 150°-155° C., contained the cis/trans isomers in a ratio of 1:3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753934
Source datasetuspto-grants-1988_06
ORD IDord-d3a7eb78bd444d0fb967eeb28ced0d84
Source noteuspto-grants-1988_06