돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 586614생성일: 2026년 10월 26일

Carbonyl bromide → 2-(4-Methylsulphinylphenyl)-1-phenyl-6,7-dihydro-5H-pyrrolizine

https://huagongshe.com/reaction/586614

반응식

참여 물질

역할이름HCID투입량
반응물Carbonyl bromideHCID 79057—
반응물5-benzyl-3,4-dihydro-2H-pyrroleHCID 224018—
반응물Sodium BicarbonateHCID 516892—
반응물4-Methylsulphinylphenacyl bromideHCID 12795537—
용매MethanolHCID 887—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Diethylether hexaneHCID 21584099—
생성물2-(4-Methylsulphinylphenyl)-1-phenyl-6,7-dihydro-5H-pyrrolizineHCID 996690912%

반응 단계

2-Benzyl-1-pyrroline (2.0 g, 80% strength, 10 mmol), dissolved in MeOH (30 ml), is treated with a solution of 4-methylsulphinylphenacyl bromide (2.1 g, 8 mmol) in CH2Cl2 (10 ml) and then with NaHCO3 (1.5 g, 18 mmol) and the mixture is stirred at RT until a TLC sample (Al2O3, hexane/ether 9:1) indicates the complete reaction of the bromoketone (Rf 0.75) and an adequate formation of product (Rf=0.2) (48 h). After addition of water (50 ml), the mixture is extracted with diethyl ether (3×30 ml), and the combined extracts are dried over Na2SO4 sicc. and concentrated. The residue is purified by CC (Al2O3, hexane/ether 1:1). 0.3 g (12%) of the compound sought is isolated.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06936632B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-3c0a79815a8b4c219fdaf96779b8c705
출처 메모uspto-grants-2005_08