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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082332Generated: November 1, 2026

4-Methylmorpholine → Cefaclor

https://huagongshe.com/reaction/1082332

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 23620956HCID 23620956—
ReactantHCID 131719758HCID 131719758—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductCefaclorHCID 5103977.3%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a mixture of 162 g of ethyl 3-α-carboxybenzylaminocrotonate potassium salt, 450 ml of dimethylformamide and 900 ml of acetonitrile, cooled to -40° C., 1.5 ml of 4-methylmorpholine and 54 ml of ethyl chloroformate are added. The mixture is stirred one hour at -40° C., then a previously cooled solution of triethylamine salt of 7-amino-3-chloro-3-cephem-4-carboxylic acid (corresponding to 99 g of free acid) in 900 ml of a mixture acetonitrile/water 1/1 (v/v) is added thereinto. The solution is kept in the cool for about 3 hours, then it is treated with 630 ml of water and filtered. The filtrate is made acid to pH 1.5 with 6N hydrochloric acid, then the pH is adjusted to 4.5 with triethyl amine. The suspension thus obtained is kept to 0° C. overnight, then it is filtered. The product thus obtained is washed with acetonitrile/water 1/1 (v/v) and dried under vacuum at 35° C. Thus, 120 g of amorphous raw cefaclor are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05589593
Source datasetuspto-grants-1996_12
ORD IDord-6ff14aa7c86445708fc5015c99517a4d
Source noteuspto-grants-1996_12