돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32195생성일: 2026년 10월 25일

Sodium Iodide → 1-(2-Fluoroethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine

https://huagongshe.com/reaction/32195

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물2-Fluoroethyl bromideHCID 12982—
반응물Sodium BicarbonateHCID 516892—
반응물1-[2-(3,3,5,5-Tetramethylcyclohexyl)phenyl]piperazineHCID 11992284—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물1-(2-Fluoroethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazineHCID 23142088—

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), 1-bromo-2-fluoroethane (16.2 mg, 0.125 mmol), sodium iodide (1.5 mg, 0.01 mmol), potassium carbonate (20.8 mg, 0.15 mmol) and dimethylformamide (1 mL) was stirred for 2 hours at an external temperature of 80° C. Saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture and extraction was performed with diethyl ether. The solvent was distilled off by nitrogen stream to the separated organic layer. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 1-(2-fluoroethyl)-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-a1af3b71c2f94d7f95a211abed352f63
출처 메모uspto-grants-2008_09