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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521481Generated: November 1, 2026

Dimethylformamide → 2-(3-Acetoxy-4-trifluoromethyl-benzoylamino)-indane-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/521481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Acetoxy-4-trifluoromethyl-benzoic acidHCID 23616794—
Reactantmethyl 2-amino-2,3-dihydro-1H-indene-2-carboxylate hydrochlorideHCID 45074056—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product2-(3-Acetoxy-4-trifluoromethyl-benzoylamino)-indane-2-carboxylic acid methyl esterHCID 6707669424%

Reaction Steps

To a solution of 2.7 g (10.9 mmol) of the compound of step 1 in 16.3 ml of a 2 M solution of oxalyl chloride in DCM (32.6 mmol), 80 mg of DMF were added and the mixture was stirred for 30 min at room temperature. The solvent was evaporated, 20 ml of DCM were added and the mixture was evaporated again. The residue was dissolved in 20 ml of DCM and the solution added within 5 min at 0° C. to a solution of 2.48 g (10.9 mmol) of 2-amino-indane-2-carboxylic acid methyl ester hydrochloride in 50 ml of DCM and 30 ml of a saturated sodium hydrogencarbonate solution. After stirring overnight, the phases were separated, the organic phase was dried over sodium sulfate, evaporated, and the residue was purified by silica gel chromatography (HEP/EA gradient). 1.1 g of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328071B2
Source datasetuspto-grants-2016_05
ORD IDord-3504f2531c1746cb9607babdcbcad2cb
Source noteuspto-grants-2016_05