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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 987021생성일: 2026년 10월 23일

Potassium Carbonate → 2,6-Bis-(1,1-dimethylethyl)-4-{[4-(4-nitrophenyl)-1-piperazinyl]-methyl}-phenol

https://huagongshe.com/ko/reaction/987021

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-(4-Nitrophenyl)piperazineHCID 80447—
반응물Phenol, 4-(bromomethyl)-2,6-bis(1,1-dimethylethyl)-HCID 612973—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2,6-Bis-(1,1-dimethylethyl)-4-{[4-(4-nitrophenyl)-1-piperazinyl]-methyl}-phenolHCID 283866154.3%

반응 단계

In a 100 ml flask containing a solution of 2.99 g (10 mmoles) of 2,6-bis-(1,1-dimethylethyl)-4-bromomethylphenol in 30 ml of DMF, 1.38 g (10 mmoles) of potassium carbonate and 2.07 g (10 mmoles) of 1-(4-nitrophenyl)piperazine are added successively. After agitation for two hours at ambient temperature, the reaction medium is diluted with 150 ml of dichloromethane and washed successively with 3×40 ml of water followed by 40 ml of brine. The organic solution is dried over sodium sulphate, filtered and concentrated under reduced pressure. The brown residue obtained is purified on a silica gel column (eluant: petroleum ether (B.p. 40-70° C.)/ethyl acetate: 8/2). After concentration of the pure fractions, 2.31 g (54%) of a brown powder is obtained. Melting point: 177.5-178.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06630461B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-a0ac114d0298493cadc1b6f07edbcac3
출처 메모uspto-grants-2003_10