HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223419Generated: October 30, 2026
Dimethylformamide → HCID 14277601, compound
https://huagongshe.com/reaction/223419
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 13180403 | HCID 13180403 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14277601 | HCID 14277601 | 88.1% |
Reaction Steps
To N,N-dimethylformamide (20 ml) were added thiourea (0.76 g), zinc powder (0.5 g) and a solution of ammonium chloride (0.67 g) in water (3 ml). To the mixture was added benzhydryl 7-phenylacetamido-3-chloromethyl-3-cephem-4-carboxylate (2.67 g) under cooling to -15° C. with stirring, and the mixture was stirred for an hour at -15° to -10° C., and then filtered. To the filtrate were added ethyl acetate (100 ml) and water (100 ml), and the organic layer was separated therefrom. The organic layer was washed with water, dried over magnesium sulfate and then concentrated under reduced pressure. The residue was pulverized with diisopropyl ether to give benzhydryl 7-phenylacetamido-3-methylenecepham-4-carboxylate (2.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04354022 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-923c6fad3e264f3799af96754fe924ad |
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| Source note | uspto-grants-1982_10 |
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