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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127653생성일: 2026년 10월 25일

N,N-Dimethylaniline → HCID 178429631, 화합물

https://huagongshe.com/reaction/127653

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물DichlorodimethylsilaneHCID 6398—
반응물Phosphorus pentachlorideHCID 24819—
반응물HCID 178429632HCID 178429632—
용매1-ButanolHCID 263—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물HCID 178429631HCID 178429631—

반응 조건

온도-20 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04256739
출처 데이터셋uspto-grants-1981_03
ORD IDord-fc782fc3eefe4c5ba419988ea529d6ea
출처 메모uspto-grants-1981_03