HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075995Generated: October 31, 2026
Dimethyl Sulfoxide → 2,2,2-Trichloroethyl 3-hydroxy-3-methyl-7-(2-phenylacetamido)cepham-4-carboxylate
https://huagongshe.com/reaction/1075995
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate | HCID 12895262 | — |
| Catalyst | Silver tetrafluoroborate | HCID 159722 | — |
| Product | 2,2,2-Trichloroethyl 3-hydroxy-3-methyl-7-(2-phenylacetamido)cepham-4-carboxylate | HCID 70590457 | 58% |
Reaction Steps
2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate (0.54 g) was dissolved in absolute dimethylsulfoxide (5 ml). To this solution was added silver fluoroborate (0.20 g) and then the mixture was stirred under shielding from light for 3 hours at room temperature. To the solution was added a solution of triethylamine (0.1 g) in dimethylsulfoxide (0.5 ml) and the solution was further stirred for 5 hours and then allowed to stand overnight at room temperature. Precipitates were filtered off and the filtrate was poured into ice-water and then extracted with ethyl acetate. The extract was washed with water and dried. The residue obtained by distilling off the solvent under reduced pressure was crystallized by a small amount of ether to give colorless crystals of 2,2,2-trichloroethyl 3-hydroxy-3-methyl-7-(2-phenylacetamido)cepham-4-carboxylate (280 mg) (58 %). This substance was recrystallized from a mixed solvent of benzene-n-hexane to give colorless needles melting at 169° to 171°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03954732 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-75c014d0cfd04ec695e4bb5052ee30dc |
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| Source note | uspto-grants-1976_05 |
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