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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465173Generated: October 30, 2026

Dimethyl Sulfate → HCID 12784140, compound

https://huagongshe.com/reaction/465173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium BicarbonateHCID 516893—
Reactant7beta-Phenoxyacetamido-3-hydroxy-3-cephem-4-carboxylic acid p-nitrobenzyl esterHCID 54716794—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 12784140HCID 12784140—

Reaction Steps

(ai) A suspension of 4.85 g of 7β-phenoxyacetamido-3-hydroxy-3-cephem-4-carboxylic acid p-nitrobenzyl ester in 25 ml of carbon tetrachloride and 27 ml of water is treated, at 20°, whilst stirring vigorously, successively with 3.0 g of potassium bicarbonate, 3.8 ml of dimethyl sulphate and 1.93 g of tetrabutylammonium bromide. The mixture is stirred vigorously for 4 hours at 20°. After diluting with 50 ml of water, the mixture is extracted with twice 50 ml of methylene chloride. 7β-Phenoxyacetamido-3-methoxy-3-cephem-4-carboxylic acid p-nitrobenzyl ester is obtained by evaporating the extracts, previously dried over sulphate, and crystallising the residue from methylene chloride/diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04550162
Source datasetuspto-grants-1985_10
ORD IDord-2c00d1cd08604aaa982347fca73fed1b
Source noteuspto-grants-1985_10