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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712647Generated: November 3, 2026

Methyl iodide → Methyl 1-(diphenylmethyl)azetidine-3-carboxylate

https://huagongshe.com/reaction/1712647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Diphenylmethyl)azetidine-3-carboxylic acidHCID 2735440—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-(diphenylmethyl)azetidine-3-carboxylateHCID 275984280.8%

Reaction Steps

Potassium carbonate (6.53 g) and iodomethane (0.976 ml) were added to a solution of 1-benzhydrylazetidine-3-carboxylic acid (4.20 g) in N,N-dimethylformamide (45 ml), followed by stirring at room temperature for 20.5 hours. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent; heptane:ethyl acetate=5:1, then 3:1). The fractions containing the target compound were concentrated to give the title compound (3.57 g, 80.8%) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790885B2
Source datasetuspto-grants-2010_09
ORD IDord-6c026da0dee645b797f0fbbdc1470e4e
Source noteuspto-grants-2010_09