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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080563Generated: November 4, 2026

Trifluoroacetic acid → HCID 67110747, compound

https://huagongshe.com/reaction/2080563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67111501HCID 67111501—
SolventDichloromethaneHCID 6344—
ProductHCID 67110747HCID 6711074775.4%

Reaction Steps

0.800 g of tert-butyl[2-(3,5-dichloropyridin-2-yl)cyclopropyl](2-iodobenzoyl)carbamate (0.00075 mol) are dissolved in 7 ml of dichloromethane. 0.70 ml of trifluoroacetic acid are added to the reaction mixture which is left stirring at room temperature overnight. The reaction mixture is quenched with 15 ml of an aqueous solution of saturated sodium bicarbonate. After separation, the aqueous phase is extracted with dichloromethane (10 ml). The combined organic phases are dried over magnesium sulfate, filtered, concentrated to dryness and purified on silica to yield to 245 mg of N-[2-(3,5-dichloropyridin-2-yl)cyclopropyl]-2-iodobenzamide (65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932396B2
Source datasetuspto-grants-2011_04
ORD IDord-a97ef9406a6e4067b4428fbf0f4b540a
Source noteuspto-grants-2011_04