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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261201Generated: November 1, 2026

Sodium hydride → HCID 68774932, compound

https://huagongshe.com/reaction/2261201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 8713889HCID 8713889—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 68774932HCID 68774932—

Reaction Steps

To a solution of N-(3-bromophenyl)-2,6-difluorobenzamide in 200 mL of DMF at room temperature and under nitrogen atmosphere, NaH 60% in oil dispersion (104.7 mmol) is slowly added and the reaction mixture is stirred for 30 minutes. Tert-butylbromoacetate (104.7 mmol) is added and the reaction stirred at room temperature. After 12 hours the reaction is complete by TLC (hexanes:ethyl acetate=8:2) and analytical LCMS (20 to 100% CH3CN). Ethyl acetate and water are added to the reaction mixture and the phases are separated. The organic phase is dried on sodium sulfate, filtered and the solvent is evaporated. The crude is purified by automated column chromatography (gradient of hexanes and ethyl acetate) to give tert-butyl 2-(N-(3-bromophenyl)-2,6-difluorobenzamido)acetate: 1H NMR (400 MHz, CDCl3) δ 7.36 (bs, 1H), 7.20 (m, 1H), 7.07 (m, 2H), 6.96 (t, J=8 Hz, 1H), 6.62 (td, J=8 Hz, J2=1.2 Hz), 4.32 (s, 2H), 1.39 (s, 9H); MS: (ES+) 448.0 (M+23)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846949B2
Source datasetuspto-grants-2010_12
ORD IDord-ccae709e33004cea8f7c87c1bb7ef06d
Source noteuspto-grants-2010_12