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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Phosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl ester | HCID 11207805 | — |
| Reactant | 4-Amino-3,4',5-trichlorobenzophenone | HCID 13373314 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04753934 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-d3a7eb78bd444d0fb967eeb28ced0d84 |
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| Source note | uspto-grants-1988_06 |
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