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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32199생성일: 2026년 10월 23일

Allyl bromide → 1-Allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine

https://huagongshe.com/ko/reaction/32199

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물Potassium CarbonateHCID 11430—
반응물Sodium BicarbonateHCID 516892—
반응물1-[2-(3,3,5,5-Tetramethylcyclohexyl)phenyl]piperazineHCID 11992284—
용매DimethylformamideHCID 6228—
용매Dichloromethane ethylacetateHCID 21226138—
생성물1-Allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazineHCID 23141803—

반응 조건

온도80 °C

반응 단계

A mixture of 1-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine (30 mg, 0.1 mmol) produced in Example (8b), allyl bromide (14.8 mg, 0.12 mmol), potassium carbonate (20.8 mg, 0.15 mmol) and dimethylformamide (1 mL) was stirred for 4 hours and 20 minutes at an external temperature of 80° C. Saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture and extraction was performed with ethyl acetate-dichloromethane. The separated organic layer was washed with water, and then the solvent was distilled off by nitrogen stream. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 1-allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425554B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-00d379097aaf48f39b85028bf376efd8
출처 메모uspto-grants-2008_09