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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716345Generated: November 3, 2026

Trifluoroacetic acid → HCID 12069573, compound

https://huagongshe.com/reaction/1716345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12069571HCID 12069571—
SolventDichloromethaneHCID 6344—
SolventDiisopropyl EtherHCID 7914—
ProductHCID 12069573HCID 1206957387%

Reaction Conditions

Temperature0 °C

Reaction Steps

2.32 ml of trifluoroacetic acid are added dropwise to a solution of 643 mg (1.51 mmol) of tert-butyl 3-(3-methoxy-4-nitrobenzoyl)-2-methylindolizin-1-ylcarbamate in 20 ml of dichloromethane, cooled to 0° C. Once the introduction is complete, the medium is allowed to return to room temperature and it is stirred for 4 hours. The reaction medium is poured over a saturated aqueous potassium carbonate solution and extracted with ethyl acetate. The organic phase is separated after settling out, washed with a saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated under reduced pressure. The crystals obtained are taken up in isopropyl ether, filtered off, washed with isopropyl ether and then dried. 425 mg of a brown solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803811B2
Source datasetuspto-grants-2010_09
ORD IDord-82adede422d448ecba01a35e126f38e2
Source noteuspto-grants-2010_09