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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851587Generated: October 25, 2026

N,N-Dimethylaniline → HCID 131711252, compound

https://huagongshe.com/reaction/851587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantTriethylamineHCID 8471—
Reactant2,2,2-Trichloroethyl 2-methyl-7-amino-3-cephem-4-carboxylate hydrochlorideHCID 12834135—
ReactantBenzylthiocarbonyl chlorideHCID 19906501—
SolventDichloromethaneHCID 6344—
ProductHCID 131711252HCID 13171125290.2%

Reaction Conditions

Temperature-15 °C

Reaction Steps

2,2,2-Trichloroethyl 2-methyl-7-amino-3-cephem-4-carboxylate hydrochloride (3.0 g) was suspended in dried dichloromethane (50 ml) and then dissolved by adding triethylamine (0.72 g) and dimethylaniline (1.9 g) under cooling at -15° C. To a mixture was dropwise added a solution of phenylthioacetyl chloride (2.2 g) in dried dichloromethane (10 ml) under stirring, and the mixture was stirred for 1.5 hours at the same temperature. After the reaction, the reaction mixture was in turn washed with 5% hydrochloric acid, water, 5% sodium bicarbonate aqueous solution and water and then dried. After the solvent was distilled off, ether was added to the residue, after which the precipitated crystals were collected by filtration and dried to give 2,2,2-trichloroethyl 2-methyl-7-(2-phenylthioacetamido)-3-cephem-4-carboxylate (3.4 g), mp 140° to 142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04385176
Source datasetuspto-grants-1983_05
ORD IDord-dcc77b214b0f4656adb3610d244174a5
Source noteuspto-grants-1983_05