Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46458Generated: October 28, 2026

Methyl iodide → 1-Benzhydryl-2-(alpha-methylaminobenzyl)azetidine

https://huagongshe.com/reaction/46458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzhydryl-2-(alpha-aminobenzyl)azetidineHCID 20345273—
SolventDimethylformamideHCID 6228—
Product1-Benzhydryl-2-(alpha-methylaminobenzyl)azetidineHCID 20345287—

Reaction Conditions

Temperature-25 °C

Reaction Steps

To a stirred solution of 2.50 g of 1-benzhydryl-2-(α-aminobenzyl)azetidine in 25 ml. of N,N-dimethylformamide, add 365 mg. of a 55% dispension of sodium hydride. Stir the mixture under a nitrogen atmosphere and when frothing subsides, warm and maintain the stirred mixture at 40° for twenty minutes. Cool the mixture to -25° C. and add 1.20 g. of methyl iodide. Remove the reaction mixture from the cooling bath and allow it to warm to room temperature. After ca. 15 minutes at room temperature, pour the contents of the reaction flask into a stirred mixture of 100 ml. of water and 25 ml. of ether. Separate the layers and re-extract the aqueous phase with ether. Combine all ether extracts, wash successively with water and brine, dry over anhydrous sodium sulfate, and strip off solvent in vacuo. Crystallize the residual solid from ether to obtain the analytically pure title compound containing 1/4 mole of water-of-crystallization and having m.p. 111°-113°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04173566
Source datasetuspto-grants-1979_11
ORD IDord-51470e56aa694d6d91b1a84d675157ce
Source noteuspto-grants-1979_11