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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765828Generated: October 30, 2026

Methyl iodide → 4-Bromo-2-[(cyclopropyl-methylamino)-methyl]-benzoic acid isopropyl ester

https://huagongshe.com/reaction/1765828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-cyclopropylaminomethyl-benzoic acid isopropyl esterHCID 57424253—
SolventAcetoneHCID 180—
Product4-Bromo-2-[(cyclopropyl-methylamino)-methyl]-benzoic acid isopropyl esterHCID 5742425488.5%

Reaction Steps

A solution of 4-bromo-2-cyclopropylaminomethyl-benzoic acid isopropyl ester (Intermediate 119, 1.33 g, 4.26 mmol) in acetone (8 mL) was treated with potassium carbonate (2.36 g, 17.05 mmol) and methyl iodide (0.53 mL, 8.52 mmol) and the resulting reaction mixture was stirred at ambient temperature for 3 h. The volatiles were evaporated in vacuo, the residue was diluted with water and extracted with diethyl ether (×2). The combined organic phase was dried over anhydrous magnesium sulfate, filtered over a short bed of silica gel (230–400 mesh) and evaporated in vacuo to afford the title product (1.23 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226951B2
Source datasetuspto-grants-2007_06
ORD IDord-9b267b4302c14901b21133e1bb140f03
Source noteuspto-grants-2007_06