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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196380Generated: October 31, 2026

o-Benzylbenzoic acid → 2-benzyl-N-methylbenzamide

https://huagongshe.com/reaction/2196380

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Benzylbenzoic acidHCID 11924—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantMethylamine hydrochlorideHCID 6364545—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-benzyl-N-methylbenzamideHCID 412850944,856.801%

Reaction Steps

To a stirred solution of α-phenyl-o-toluic acid (2.0 g, 9.43 mmol) in methylene chloride (500 mL) at room temperature under argon was added by dropwise addition a solution of oxalyl chloride (0.988 mL, 11.3 mmol) in methylene chloride (50 mL). N,N-Dimethylformamide (10 drops) were added and the contents of the reaction flask were stirred 1.5 h. Solvent was removed in vacuo and methylene chloride (100 mL) and methylamine hydrochloride (950 mg, 14.1 mmol) was added. With ice-bath cooling a solution of N,N-diisopropylethylamine (4.10 mL, 23.6 mmol) in methylene chloride (10 mL) was added dropwise. Saturated sodium bicarbonate was added and the resulting mixture extracted with methylene chloride (3×). The combined organic extracts were dried with sodium sulfate (anh.). Filtration followed by removal of the solvent in vacuo gave a solid which after trituration with ether afforded N-Methyl-2-(phenylmethyl)benzamide (974 mg, 4.23 mol, 46%). MS [M+H]+ 226

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338449B2
Source datasetuspto-grants-2012_12
ORD IDord-4e051715dadc4ef7b90058ce0d540bb4
Source noteuspto-grants-2012_12