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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660597Generated: November 3, 2026

N,N-Dimethylaniline → HCID 12833985, compound

https://huagongshe.com/reaction/1660597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantTriethylamineHCID 8471—
Reactant2-Thiopheneacetyl chlorideHCID 162362—
Reactant2,2,2-Trichloroethyl 2-methyl-7-amino-3-cephem-4-carboxylate hydrochlorideHCID 12834135—
SolventDichloromethaneHCID 6344—
ProductHCID 12833985HCID 1283398586.8%

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 solution was dropwise added a solution of (2-thienyl)acetyl chloride (2.0 g) in dried dichloromethane (10 ml) under stirring and cooling at the same temperature, 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, the residue was dissolved in ether, allowed to stand, after which the precipitated crystals were collected by filtration and dried to give crystals of 2,2,2-trichloroethyl 2-methyl-7-[2-(2-thienyl)acetamido]-3-cephem-4-carboxylate (3.2 g), mp 161° to 162° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308380
Source datasetuspto-grants-1981_12
ORD IDord-b543efc7f26d45488ac5ed1e926b675a
Source noteuspto-grants-1981_12