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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057605Generated: November 3, 2026

Hydrochloric Acid → 3-Acetoxymethyl-7-amino-3cephem-4-carboxylic acid

https://huagongshe.com/reaction/2057605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantN,N-DiethylanilineHCID 7061—
ReactantTriphenyl phosphiteHCID 7540—
ReactantChlorineHCID 24526—
ReactantCephalosporin CHCID 65536—
ReactantSodiumHCID 5360545—
CatalystTriphenyl phosphiteHCID 7540—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventIsobutanolHCID 6560—
Product3-Acetoxymethyl-7-amino-3cephem-4-carboxylic acidHCID 1134631083%

Reaction Conditions

Temperature-35 °C

Reaction Steps

4.8 gm (10 mmol) of cephalosporin C, sodium salt, dihydrate was suspended in 80 ml of methylene chloride (cyclohexane stabilized, dried over 4A molecular sieves). Diethyl aniline (dried over KOH), 7.4 gm (8 ml, 50 mmol), and acetyl chloride, 4.7 gm (4.3 ml, 60 mmol), were added. The mixture was stirred in an ice bath at 30° to 40° C. for 1 hour and then at room temperature for 2 hours. Filtration removed 1.65 gm of undissolved material. The reaction solution was cooled in an ice-alcohol bath before addition to a solution of the triphenyl phosphite-chlorine kinetic compound prepared as follows: triphenyl phosphite, 6.8 gm (5.8 ml, 22 mmol), was added to 100 ml of dry methylene chloride and cooled to ice-alcohol temperature before the addition of chlorine gas until a yellow coloration persisted. The addition of a few drops of triphenyl phosphite gave a colorless solution. After mixing the two above described solutions at ice alcohol temperature, diethyl aniline, 3.3 gm (3.5 ml, 22 mmol), in 20 ml of dry methylene chloride was added dropwise over a period of 10 minutes. The reaction mixture was stirred in the cold for 2 hours, then cooled further to about -35° C. and treated with isobutanol (dried over 3A molecular sieves), 6.0 gm (7.4 ml, 80 mmol). A stream and dry hydrogen chloride was then passed through the reaction mixture for about 30 seconds. The reaction mixture was refrigerated overnight. Twenty ml of water was then added to the methylene chloride solution. The resulting 2-phase mixture was stirred vigorously for 5 minutes. The methylene chloride layer was separated and washed with 20 ml of water. The aqueous layer and the aqueous wash were combined, washed with ethyl acetate and then adjusted to pH 3.8 with saturated ammonium bicarbonate solution. After 30 minutes at ice bath temperature the aqueous slurry was filtered to provide 1.5 gm (vacuum dried, 83%) of 7-ACA.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04211702
Source datasetuspto-grants-1980_07
ORD IDord-1d65db9d0f2f4f6894b779cadb4d373c
Source noteuspto-grants-1980_07