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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283146Generated: October 31, 2026

Ammonia → HCID 11391647, compound

https://huagongshe.com/reaction/1283146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantChloroformHCID 6212—
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantHCID 13127405HCID 13127405—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 11391647HCID 1139164796.2%

Reaction Steps

Diphenylmethyl (6R,7R)-7-amino-3-carbamoyloxymethylceph-3-em-4-carboxylate toluene-p-sulphonic acid salt (300.0 g, 0.44 mole), solvated with ca. 0.6 mole of chloroform, was added in portions over 30 minutes to a stirred mixture of trifluoroacetic acid (300 ml) and anisole (300 ml) immersed in a water-bath at 20°. The temperature of the mixture rose from 23° to 28° over the first 20 minutes but fell back to 26° by the end of the addition. The golden yellow solution was stirred for 1 hour, the temperature falling to 21°, and was then added to a stirred mixture of ethyl acetate (1.5 liters) and water (1.5 liters) immersed in an ice-bath. The pH of the stirred mixture was adjusted to 3.8 over 10 minutes with ammonia solution (S.G. 0.880), the temperature rising to 38°. The suspension was stirred and cooled to 10° over 1.25 hours and filtered. The cream solid was washed with water (750 ml) and ethyl acetate (4 × 200 ml) and dried in vacuo to give the title compound (115.6 g, 96.2%); λmax (pH6 phosphate) 265nm (ε7,750); purity by HPLC (high pressure liquid chromatography) 99.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03974153
Source datasetuspto-grants-1976_08
ORD IDord-b272c3f8b7524dbab6e2bf8cef5ad7d2
Source noteuspto-grants-1976_08