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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 426952생성일: 2026년 10월 24일

Nitromethane → 1-p-Fluorobenzyl-2-nitromethylene-pyrrolidine

https://huagongshe.com/reaction/426952

반응식

참여 물질

역할이름HCID투입량
반응물NitromethaneHCID 6375—
반응물Dimethyl SulfateHCID 6497—
반응물2-Pyrrolidinone, 1-((4-fluorophenyl)methyl)-HCID 3045446—
반응물SodiumHCID 5360545—
반응물Sodium MethoxideHCID 10942334—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물1-p-Fluorobenzyl-2-nitromethylene-pyrrolidineHCID 5400911155.2%

반응 조건

온도50 °C

반응 단계

26.1 g (0.207 mol) of dimethyl sulphate are added to 40 g (0.207 mol) of 1-p-fluorobenzyl-pyrrolidin-2-one and the mixture is heated to 60° for 4 hours. It is then cooled and a solution of sodium methylate prepared from 4.75 g (0.207 gram atom) of sodium and 100 ml of methanol is introduced slowly, at 0°. When the addition is complete, the mixture is stirred for 30 minutes at 50° C. and again cooled to 0°, and 18.9 g (0.31 mol) of nitromethane are added dropwise whilst continuing the stirring. The reaction mixture is left at ambient temperature for 12 hours and is then heated to 50° for 2 hours. It is cooled, and poured into 500 ml of water, which are then extracted with chloroform. The organic layer is now separated off, washed with water and dried over magnesium sulphate, and the solvent is driven off. The residual product is washed with ether and recrystallised from ethanol. 27 g (55.2% yield) of 1-p-fluorobenzyl-2-nitromethylene-pyrrolidine are thus collected in the form of light yellow crystals melting at 108.5°-109°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04172143
출처 데이터셋uspto-grants-1979_10
ORD IDord-d0cfedf70e894672bed7d8a50dcaf016
출처 메모uspto-grants-1979_10