돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35340생성일: 2026년 10월 24일

Potassium Iodide → N-(2,6-dimethylphenyl)-2-(1-hydroxyethyl)-4-(phenylmethyl)-1-piperazineacetamide

https://huagongshe.com/ko/reaction/35340

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium CarbonateHCID 10340—
반응물2-Chloro-N-(2,6-dimethylphenyl)acetamideHCID 70798—
반응물alpha-Methyl-4-(phenylmethyl)-2-piperazinemethanolHCID 14230267—
용매DimethylformamideHCID 6228—
생성물N-(2,6-dimethylphenyl)-2-(1-hydroxyethyl)-4-(phenylmethyl)-1-piperazineacetamideHCID 1423022284.8%

반응 조건

온도60 °C

반응 단계

A mixture of 24.0 parts of α-methyl-4-(phenylmethyl)-2-piperazinemethanol, 27.3 parts of 2-chloro-N-(2,6-dimethylphenyl)acetamide, 25.4 parts of sodium carbonate, 0.1 parts of potassium iodide and 180 parts of N,N-dimethylformamide was stirred for 18 hours at 60° C. The reaction mixture was poured onto water and the product was extracted with dichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 1,1'-oxybisethane, yielding 35.19 parts (84.8%) of N-(2,6-dimethylphenyl)-2-(1-hydroxyethyl)-4-(phenylmethyl)-1-piperazineacetamide; mp. 148.8° C. (compound 113).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766125
출처 데이터셋uspto-grants-1988_08
ORD IDord-75fdca07dd8d42d88dc2c02046d78d62
출처 메모uspto-grants-1988_08