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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 458892생성일: 2026년 10월 26일

Dimethylformamide → 9H-Xanthene-9-carboxylic acid (3R)-1-methylpyrrolidin-3-yl ester

https://huagongshe.com/reaction/458892

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물Xanthene-9-carboxylic acidHCID 65736—
반응물1-Methyl-3-pyrrolidinol, (-)-HCID 6951332—
용매ChloroformHCID 6212—
생성물9H-Xanthene-9-carboxylic acid (3R)-1-methylpyrrolidin-3-yl esterHCID 8660225893%

반응 조건

온도0 °C

반응 단계

2 g of 9H-Xanthene-9-carboxylic acid (0.0088 mol) were dissolved in 30 ml of CHCl3 (ethanol free). The solution was cooled at 0° C. and 1.08 ml (0.0123 mol) of oxalyl chloride and a drop of DMF was added. The mixture was stirred and allowed to warm to room temperature. After an hour at this temperature the solvents were evaporated and the residue was dissolved in CHCl3 and evaporated again. This procedure was repeated two times. The solid obtained (2.19 g) was dissolved in 20 ml of CHCl3 and added to a solution of 0.975 g (0.0097 mol) of (3R)-1-methylpyrrolidin-3-ol (Intermediate I-19) in 15 ml of CHCl3 cooled at 0–5° C. The reaction mixture was allowed to warm to room temperature and stirred overnight. The solvent was evaporated and the residue was dissolved in toluene and extracted with HCl 2N. The aqueous layer was basified with K2CO3 and extracted with CHCl3. The organic layer was washed with brine, dried over Na2SO4 and evaporated to dryness to yield 2.53 g (93%) of the title product as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192978B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-2d3ecfc79f2d4888bf50706c464f5c8f
출처 메모uspto-grants-2007_03