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HRID 458892作成日:2026年10月26日

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

https://huagongshe.com/reaction/458892

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物Xanthene-9-carboxylic acidHCID 65736—
反応物1-Methyl-3-pyrrolidinol, (-)-HCID 6951332—
溶媒ChloroformHCID 6212—
生成物9H-Xanthene-9-carboxylic acid (3R)-1-methylpyrrolidin-3-yl esterHCID 8660225893%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07192978B2
出典データセットuspto-grants-2007_03
ORD IDord-2d3ecfc79f2d4888bf50706c464f5c8f
出典メモuspto-grants-2007_03