HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463156Generated: November 1, 2026
Chlorotrimethylsilane → HCID 88720763, compound
https://huagongshe.com/reaction/1463156
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Reactant | (6R)-7-amino-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid | HCID 13475828 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 88720763 | HCID 88720763 | — |
Reaction Steps
To a suspension of 7-amino-3-methylceph-3-em-4-carboxylic acid (7.76 g., 0.036 mole) in anhydrous THF at 0°, cooled in an ice-bath, was added trimethylchlorosilane (7.8 g., 9.07 ml., 2 equivalents) and triethylamine (7.3 g., 10 ml., 2 equivalents). After 10 minutes the ice-bath was removed and the mixture left at ambient temperature for 2 hours. To the mixture was added two equivalents of acetic formic mixed anhydride and the mixture was allowed to stand at ambient temperature for a further 1.5 hours. Water (5 ml.) was added, the precipitated triethylamine hydrochloride was filtered off and the filtrate evaporated on a rotatory evaporator. THF (50 ml.) was added to the residual oil and the solution was esterified with diphenyldiazomethane. The product was purified by chromatography on silica using CH2Cl2 /ether 1:1 v/v as eluant to give diphenylmethyl 7-formylamino-3-methylceph-3-em-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04463173 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-338abc36e7e5410eba4ae44652eeecc6 |
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| Source note | uspto-grants-1984_07 |
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