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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154542Generated: October 31, 2026

Triphenyl phosphite → HCID 131714070, compound

https://huagongshe.com/reaction/1154542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenyl phosphiteHCID 7540—
ReactantChlorineHCID 24526—
ReactantN,N-Bis(trimethylsilyl)trifluoroacetamideHCID 65279—
Reactant(6R)-7-amino-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 13475828—
ReactantHCID 54527833HCID 54527833—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 131714070HCID 131714070—

Reaction Conditions

Temperature25 °C

Reaction Steps

Four hundred twenty milligrams of α-methoxyimino-α-(8-chloro-2-naphthyl)acetic acid were converted to the acid chloride by reaction with excess chlorine and 500 mg of triphenyl phosphite in 20 ml of dichloromethane. The reaction mixture was added in one portion to a stirred solution of 350 mg of 7-amino-3-methyl-3-cephem-4-carboxylic acid in 5 ml of dichloromethane containing 2 ml of bis(trimethylsilyl)trifluoroacetamide. The reaction mixture was stirred at 25° C. for six hours and then diluted by addition of 20 ml of methanol. The solvent was removed by evaporation under reduced pressure to provide 7-[α-methoxyimino-α-(8-chloro-2-naphthyl)acetamido]-3-methyl-3-cephem-4-carboxylic acid. The product thus formed is dissolved in formic acid containing zinc metal dust to give, following isolation and purification, 7-(8-chloro-2-naphthyl)glycylamido-3-methyl-3-cephem-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490370
Source datasetuspto-grants-1984_12
ORD IDord-839a6f8a1a11409e97f40071c2a77230
Source noteuspto-grants-1984_12