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HRID 127653作成日:2026年10月26日

N,N-Dimethylaniline → HCID 178429631、化合物

https://huagongshe.com/reaction/127653

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylanilineHCID 949—
反応物DichlorodimethylsilaneHCID 6398—
反応物Phosphorus pentachlorideHCID 24819—
反応物HCID 178429632HCID 178429632—
溶媒1-ButanolHCID 263—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒1,4-DioxaneHCID 31275—
生成物HCID 178429631HCID 178429631—

反応条件

温度-20 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04256739
出典データセットuspto-grants-1981_03
ORD IDord-fc782fc3eefe4c5ba419988ea529d6ea
出典メモuspto-grants-1981_03