HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436272Generated: October 30, 2026
Isobutyric Acid → HCID 131710653, compound
https://huagongshe.com/reaction/436272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyric Acid | HCID 6590 | — |
| Reactant | Propyl mercaptan | HCID 7848 | — |
| Reactant | HCID 178526147 | HCID 178526147 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 131710653 | HCID 131710653 | — |
Reaction Steps
To 0.391 g. (1 mmol.) of mercuric acetate in a mixture of 15 ml. of toluene and 15 ml. of isobutyric acid are added 0.739 g. (1 mmol.) of 3-hydroxy-4 -bromo-2-[2-formylthio-4-oxo-3-(α-benzhydryloxycarbonylphenylacetamido)-1-azetidinyl]-2-butenoate, benzhydryl ester, as a neat solid. The mixture is stirred for 20 minutes at 18° C., after which time the solution becomes cloudy. n-Propyl mercaptan is added to the mixture, and the mixture then is filtered through activated charcoal and a filter aide. The resulting filtrate is evaporated, and a residue comprising benzhydryl 7-(α-benzhydryloxycarbonylphenylacetamido)-3-hydroxy-3-cephem-4-carboxylate is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04008230 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-2c6d5a9325cf4bac8e10e0496bba2fa0 |
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| Source note | uspto-grants-1977_02 |
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