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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725508Generated: October 27, 2026

Dimethylformamide → Tert-butyl 4-(2-fluoro-3-formylbenzoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1725508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 4-(3-bromo-2-fluorobenzoyl)piperazine-1-carboxylateHCID 57562603—
ReactantHCID 178418368HCID 178418368—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(2-fluoro-3-formylbenzoyl)piperazine-1-carboxylateHCID 57562639—

Reaction Steps

194 mg of tert-butyl 4-(3-bromo-2-fluorobenzoyl)piperazine-1-carboxylate was dissolved in 5.0 ml of tetrahydrofuran, and 1.25 ml of a solution of isobutylmagnesium chloride in tetrahydrofuran (2.0 M) was added thereto at −78° C. After stirring at the same temperature for 2 hours, 0.39 ml (5.0 mmol) of N,N-dimethylformamide was added thereto. The resulting mixture was stirred at the same temperature for 30 minutes and further stirred at 0° C. for 30 minutes. To the reaction mixture was added saturated ammonium chloride, and the mixture was extracted with chloroform. The organic layer was washed with brine and then concentrated. The residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate=9/1 to 1/1) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491720B2
Source datasetuspto-grants-2009_02
ORD IDord-38054f819b814ab2a2456e7d7eec6692
Source noteuspto-grants-2009_02