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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223621Generated: October 28, 2026

Methanol → HCID 178477374, compound

https://huagongshe.com/reaction/223621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyridineHCID 1049—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantHCID 178477370HCID 178477370—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178477374HCID 17847737464%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a suspension of 6.25 g of phosphorus pentachloride in 45 ml of anhydrous methylene chloride cooled at -10° C., is added 20 ml of anhydrous methylene chloride solution containing 2.4 g of pyridine and the mixed solution is stirred for 30 minutes. To the solution is dropwise added a solution of 9.3 g of 7β-(2-thienylacetamido)-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid benzhydryl ester in 30 ml of anhydrous methylene chloride during 30 minutes under stirring and keeping at -20° C.--10° C. The mixture is further stirred for 2 hours at the same temperature and then cooled to -30° C.--20° C., followed by adding dropwise 56 ml of methanol. Thus obtained solution is stirred for 30 minutes, keeping the temperature of the solution between -5° C. and 5° C., and 60 ml of water is added dropwise thereto, followed by further stirring for 30 minutes. Methylene chloride layer is washed with saturated aq. NaCl solution and concentrated. To the concentrate is added a mixture of water and ethyl acetate under stirring to give 4.746 g of 7-amino-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid benzhydryl ester as a crystal. Yield 64.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355160
Source datasetuspto-grants-1982_10
ORD IDord-3fd43e954a38450f915c4a90be267374
Source noteuspto-grants-1982_10