HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249420Generated: November 3, 2026
Hydrochloric Acid → HCID 131714996, compound
https://huagongshe.com/reaction/1249420
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 131714997 | HCID 131714997 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131714996 | HCID 131714996 | 90.1% |
Reaction Steps
To a solution of benzhydryl 7-[2-t-butoxycarbonylmethoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-[(E)-2-chlorovinyl]-3-cephem-4-carboxylate (syn isomer) (3.0 g) in a mixed solvent of methanol (30 ml) and tetrahydrofuran (5 ml) was added concentrated hydrochloric acid (1.67 ml) at room temperature, and the mixture was stirred for two hours at the same temperature. The reaction mixture was diluted with water (40 ml), adjusted to pH 6.0 with an aqueous solution of sodium bicarbonate and extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried and evaporated under reduced pressure. The residue was triturated with diisopropyl ether and collected by filtration to give benzhydryl 7-[2-t-butoxycarbonylmethoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-[(E)-2-chlorovinyl]-3-cephem-4-carboxylate (syn isomer) (2.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04631274 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-634c762893934b1881c08cda214b956e |
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| Source note | uspto-grants-1986_12 |
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