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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377418Generated: October 31, 2026

Water → 3-Bromo-N-cyclopropyl-4,N-dimethyl-benzamide

https://huagongshe.com/reaction/2377418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-bromo-N-cyclopropyl-4-methylbenzamideHCID 21107152—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-N-cyclopropyl-4,N-dimethyl-benzamideHCID 21107153—

Reaction Steps

A stirred, cooled (ice bath) solution of 3-bromo-N-cyclopropyl-4-methyl-benzamide (Intermediate 95, 6 g, 23.25 mmol) in anhydrous tetrahydrofuran (100 mL) under argon was treated with small portions of sodium hydride (1.6 g, 40 mmol, 60% dispersion in mineral oil). The reaction mixture was allowed to warm to ambient temperature and after 1 h, methyl iodide (3.11 mL, 50 mmol) was added and the reaction mixture was refluxed for 5 h. It was cooled to ambient temperature, poured into cold water and extracted with diethyl ether (×2). The combined organic phase was dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford the title product as a dirty brown solid that was used as such for the next step (6.3 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468391B2
Source datasetuspto-grants-2008_12
ORD IDord-8035f846b33d419bb7946064d97c5cb3
Source noteuspto-grants-2008_12