돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1448480생성일: 2026년 10월 26일

Sodium hydride → 1-(2-Propynyl)-4-(2-pyridinyl)-piperazine

https://huagongshe.com/reaction/1448480

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-(2-Pyridyl)piperazineHCID 94459—
반응물1-Propyne, 1-bromo-HCID 137279—
반응물SodiumHCID 5360545—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(2-Propynyl)-4-(2-pyridinyl)-piperazineHCID 10631913—

반응 조건

온도50 °C

반응 단계

Propynylbromide (11.9 g.) was added to the sodium salt of N-(2-pyridyl)piperazine prepared from 16.3 g. of N-(2-pyridyl)piperazine and 4.8 g. of sodium hydride/50% mineral oil dispersion in 50 ml. of dry dimethylformamide. The mixture was stirred at 50° C. for 3 hours and then carefully poured into 3 volumes of cold water. This mixture was extracted with several portions of either and the combined ether extracts were washed twice with 10% aqueous hydrochloric acid. The acidic extract was made strongly alkaline by adding 40% aqueous sodium hydroxide under cooling. The mixture was then extracted several times with ether and the combined extracts were dried over magnesium sulfate. The latter was then removed by filtration, and the filtrate was evaporated to produce a brown oil. Distillation under reduced pressure gave N'-(2-pyridyl)-N-(2-propynyl)piperazine, b.p. 153°-4° C./3.5 mm, as a yellow oil which showed the expected NMR and IR spectra.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04180574
출처 데이터셋uspto-grants-1979_12
ORD IDord-55aaf42d1f144f55894ab88aad3aa39c
출처 메모uspto-grants-1979_12