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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851592Generated: October 31, 2026

N,N-Dimethylaniline → HCID 12834068, compound

https://huagongshe.com/reaction/851592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
Reactantalpha-Sulfophenylacetic acidHCID 413605—
Reactant2,2,2-Trichloroethyl 2-methyl-7-amino-3-cephem-4-carboxylate hydrochlorideHCID 12834135—
ReactantHCID 21930676HCID 21930676—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 12834068HCID 12834068—

Reaction Steps

A suspension of 2,2,2-trichloroethyl-2-methyl-7-amino-3-cephem-4-carboxylate hydrochloride (6.9 g) in dried dichloromethane (70 ml) was homogenized by adding triethylamine (1.48 g) and N,N-dimethylaniline (0.44 g) under stirring and ice-cooling and by stirring for 30 minutes at room temperature. A solution of triethylamine salt of mixed anhydride of 2-sulfo-2-phenylacetic acid with ethoxycarbonic acid (8.5 g) in dried dichloromethane (60 ml) was dropwise added over about 30 minutes under stirring and cooling at -20° to -25° C. to the above-mentioned solution, and the mixture was stirred for 1.5 hours at -10° to -15° C. and for 1 hour at room temperature. After the reaction, dichloromethane was removed at low temperature, and the residue was dissolved in ethyl acetate, after which the solution was washed with cooled 5% hydrochloric acid and three times with water, and then dried. The solvent was distilled off at low temperature to give 2,2,2-trichloroethyl 2-methyl-7-(2-sulfo-2-phenylacetamido)-3-cephem-4-carboxylate (11.5 g), amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04385176
Source datasetuspto-grants-1983_05
ORD IDord-96bc49ea2e5e447ab37aae180876b4cd
Source noteuspto-grants-1983_05