돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1193548생성일: 2026년 10월 26일

Sodium hydride → 1-Acetyl-4-ethynyl-4-(2-nitrophenoxy)piperidine

https://huagongshe.com/reaction/1193548

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-Fluoro-2-nitrobenzeneHCID 73895—
반응물Methane, sulfinylbis-, ion(1-), sodiumHCID 10154010—
반응물1-(4-Ethynyl-4-hydroxypiperidin-1-yl)ethan-1-oneHCID 13216735—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물1-Acetyl-4-ethynyl-4-(2-nitrophenoxy)piperidineHCID 1428148824%

반응 단계

To a stirred solution of dimsyl sodium, prepared from 16.5 g of sodium hydride (50% in oil, washed three times with hexanes) and 400 ml of dimethylsulfoxide at 17°-25° was added, in aliquots, 57.7 g of 1-acetyl-4-ethynyl-4-piperidinol. Upon completion of the addition, 55.3 g of 2-fluoronitrobenzene was added dropwise at a rate such that the temperature remained below 25°. The mixture was stirred at room temperature for 20 min, poured into cold water, extracted three times with ether, washed with saturated sodium chloride solution and dried over anhydrous potassium carbonate. Filtration followed by evaporation of solvent provided an oil, which crystallized on standing. Recrystallization from ethyl acetate/cyclohexane provided 23.6 g (24%) of product, mp 112°-115°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04810792
출처 데이터셋uspto-grants-1989_03
ORD IDord-3ebe733b3b70488daa38ed37d48b843b
출처 메모uspto-grants-1989_03