HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659755Generated: November 2, 2026
Trifluoroacetic acid → HCID 131712592, compound
https://huagongshe.com/reaction/1659755
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131712593 | HCID 131712593 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 131712592 | HCID 131712592 | 42.8% |
Reaction Steps
Trifluoroacetic acid (20 ml) was added under ice-cooling to a stirred suspension of 7-[2-t-butoxycarbonylmethoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-(1-allyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer)(2.05 g) in anisole (2 ml), and the resultant mixture was stirred for 2 hours at ambient temperature. The reaction mixture was concentrated under reduced pressure and diethyl ether was added thereto. Precipitates were collected by filtration, washed with diethyl ether, dried and dissolved in an aqueous solution of sodium bicarbonate. An insoluble material was filtered off and the filtrate was adjusted to pH 3.2 with conc.hydrochloride acid. Precipitates were collected by filtration, washed with water and dried to give 7-[2-carboxymethoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-(1-allyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (0.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04304770 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-8a2541a44f024ef5823ed89c26c83a68 |
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| Source note | uspto-grants-1981_12 |
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