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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250675Generated: November 3, 2026

Dimethylformamide → (2,4-Difluoro-3-formyl-phenyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/250675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTert-butyl (2,4-difluorophenyl)carbamateHCID 22986665—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(2,4-Difluoro-3-formyl-phenyl)-carbamic acid tert-butyl esterHCID 58086596—

Reaction Steps

To 2,4-difluoro-phenyl)-carbamic acid tert-butyl ester (123, 1.41 g, 6.17 mmol) in tetrahydrofuran (60.0 mL) under an atmosphere of nitrogen at 78° C. were added n-butyllithium (2.50 M in hexane, 2.59 mL) for 30 min. Lithium diisopropylamide (2.0 M in hexane, 3.4 mL) was added to the reaction. After 35 min, N,N-dimethylformamide (1.05 mL, 0.0136 mol) was added to the reaction mixture. The reaction was allowed to cool to room temperature overnight. The organic layer was washed with brine, dried over sodium sulfate, concentrated and purified by silica gel chromatography, eluting with 20% ethyl acetate in hexane to provide compound 124.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863288B2
Source datasetuspto-grants-2011_01
ORD IDord-b5f51c308a444db3be8f59b8a066e16b
Source noteuspto-grants-2011_01