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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468041Generated: October 26, 2026

Trifluoroacetic acid → 2,5-Difluorobenzohydrazide

https://huagongshe.com/reaction/468041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactanttert-Butyl carbazateHCID 70091—
Reactant2,5-Difluorobenzoic acidHCID 76339—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
Product2,5-DifluorobenzohydrazideHCID 2774074—

Reaction Steps

To a solution of 2,5-difluorobenzoic acid (3.5 g, 22 mmol) in THF/DMF (20 mL/20 mL) was added EDCI (4.7 g, 24 mmol), DMAP (50 mg) and NH2NHBoc (3.07 g, 23.2 mmol). After stirring for 16 hours, the reaction was quenched with water (30 mL) and diluted with EtOAc (30 mL). The organic layer was then washed with HCl (0.5 M, 20 mL), saturated NaHCO3 (20 mL), and brine (20 mL). The organic layer was then dried over Na2SO4, filtered and concentrated under reduced pressure to afford the crude Boc-protected product, which was then dissolved in DCM (60 mL) at 0° C. TFA (50 mL) was added to the above DCM solution. After stirring for 2 hours, the reaction mixture was concentrated and the residue was dissolved in DCM (60 mL). The solution was washed with saturated NaHCO3 (40 mL) and dried over Na2SO4, filtered and concentrated under reduced pressure to afford the desired crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623895B2
Source datasetuspto-grants-2014_01
ORD IDord-737deca237754139bf70d7f4e37e762b
Source noteuspto-grants-2014_01