돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32200생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/32200

반응식

참여 물질

역할이름HCID투입량
반응물Propargyl bromideHCID 7842—
반응물Potassium CarbonateHCID 11430—
반응물Sodium BicarbonateHCID 516892—
반응물1-[2-(3,3,5,5-Tetramethylcyclohexyl)phenyl]piperazineHCID 11992284—
용매DimethylformamideHCID 6228—
용매Dichloromethane ethylacetateHCID 21226138—
생성물1-Prop-2-ynyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazineHCID 23141694—

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), propargyl bromide (14.3 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-prop-2-ynyl-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-b769cb3be73b46cb83e12c9a7ad739e9
출처 메모uspto-grants-2008_09