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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252313Generated: October 29, 2026

N,N-Dimethylaniline → HCID 178525023, compound

https://huagongshe.com/reaction/1252313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantBenzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylateHCID 13239626—
ReactantHCID 21269519HCID 21269519—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 178525023HCID 178525023—

Reaction Steps

2.12 g (3 mmol) of (Z)-2-(1-benzhydryloxycarbonyl-1-cyclopentyloxyimino)-2-(2-tritylaminothiazol-4-yl) acetic acid and 1.24 g (3 mmol) of benzhydryl 7-amino-3-chloromethyl-3-cephem-4-carboxylate were dissolved in 50 ml of methylene chloride, and 1.2 ml (9.6 mmol) of N,N-dimethylaniline was added under cooling with ice. Then, 0.29 ml (3.15 mmol) of phosphorus oxychloride was dropwise added thereto, and the mixture was stirred at the same temperature for 4 hours. 30 ml of chloroform and 30 ml of water was added to the reaction solution. The organic layer was washed with water and with a saturated sodium chloride aqueous solution, then dried over anhydrous sodium sulfate and concentrated to obtain the residue of the above identified compound, which was used for the subsequent reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742053
Source datasetuspto-grants-1988_05
ORD IDord-4af7dd36e5344caa952f181e0911c29e
Source noteuspto-grants-1988_05