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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127653Generated: October 25, 2026

N,N-Dimethylaniline → HCID 178429631, compound

https://huagongshe.com/reaction/127653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantDichlorodimethylsilaneHCID 6398—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantHCID 178429632HCID 178429632—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178429631HCID 178429631—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A suspension of 3.80 g (10 mmols) of 7β-phenoxyacetamido-3-methylthio-ceph-3-em-4-carboxylic acid in 38 ml of absolute methylene chloride is stirred with 4.45 ml of dimethylaniline and 1.50 ml of dimethyldichlorosilane for 30 minutes at room temperature. The reaction mixture is cooled to -20° C., 2.60 g of phosphorus pentachloride are added, the mixture is stirred for 30 minutes at -20° C. and is then added dropwise to a mixture, cooled to -20° C., of 15.5 ml of n-butanol and 1.47 ml of dimethylaniline. The temperature is allowed to rise to -10° C. and 15.5 ml of dioxane and 0.53 ml of water are added. When crystallisation starts, the pH value is adjusted to 4.1 with tributylamine and crystallisation is brought to completion by stirring for 2 hours at 0°-5° C. The precipitate is filtered off, washed with 10 ml of dioxane and 5 ml of methylene chloride and dried in a high vacuum. 7β-Amino-3-methylthio-ceph-3-em-4-carboxylic acid of melting point 205° C. (decomposition) is obtained; UV spectrum (0.1 N NaHCO3): λmax =293 (ε=7600); IR spectrum (nujol): characteristic bands at 3.15, 5.55 6.17 and 6.53μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256739
Source datasetuspto-grants-1981_03
ORD IDord-fc782fc3eefe4c5ba419988ea529d6ea
Source noteuspto-grants-1981_03