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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458892Generated: October 26, 2026

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

https://huagongshe.com/reaction/458892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantXanthene-9-carboxylic acidHCID 65736—
Reactant1-Methyl-3-pyrrolidinol, (-)-HCID 6951332—
SolventChloroformHCID 6212—
Product9H-Xanthene-9-carboxylic acid (3R)-1-methylpyrrolidin-3-yl esterHCID 8660225893%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192978B2
Source datasetuspto-grants-2007_03
ORD IDord-2d3ecfc79f2d4888bf50706c464f5c8f
Source noteuspto-grants-2007_03