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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868116Generated: October 31, 2026

Triethylamine → 1-Benzhydryl-N-methylazetidine-3-carboxamide

https://huagongshe.com/reaction/868116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-(Diphenylmethyl)azetidine-3-carboxylic acidHCID 2735440—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventAcetonitrileHCID 6342—
Product1-Benzhydryl-N-methylazetidine-3-carboxamideHCID 13772849114.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 7.5 g (28 mmole) of 1-(diphenylmethyl)azetidine-3-carboxylic acid in 75 ml of acetonitrile was added 6.0 g (37 mmole) of 1,1'-carbonyldiimidazole. The reaction was heated at 60° C. for two hours and successively treated with 3.11 g (30.8 mmole) of triethylamine and 2.08 g (30.8 mmole) of methylamine hydrochloride. The reaction was stirred at 60° C. for an additional hour, the solvent evaporated in vacuo, and the residue dissolved in chloroform. After washing with water and drying over magnesium sulfate, the chloroform layer was evaporated in vacuo to give 9.0 g of 1-(diphenylmethyl)-N-methyl-3-azetidinecarboxamide, mp 103°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04777175
Source datasetuspto-grants-1988_10
ORD IDord-eb4c3939f6e24da6abac1852b52814dd
Source noteuspto-grants-1988_10