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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066906Generated: October 30, 2026

Water → (1-Benzhydryl-azetidin-3-yl)-(2-methoxy-phenyl)-methyl-amine

https://huagongshe.com/reaction/1066906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxy-N-methylanilineHCID 2759579—
Reactant1-Benzhydryl-3-(methylsulfonyl)azetidineHCID 15521969—
SolventAcetonitrileHCID 6342—
Product(1-Benzhydryl-azetidin-3-yl)-(2-methoxy-phenyl)-methyl-amineHCID 2119680625.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 0.65 g of N-methyl o-anisidine in 15 mL of acetonitrile, was added 0.280 g of K2CO3, followed by 0.650 g of 1-(diphenylmethyl)-3-methane sulfonyl azetidine. The reaction mixture was heated at 80° C. for 1 h then at 50° C. overnight. Water was added and the mixture was extracted with ether. The organic phase was dried and the solvent was removed under vacuo. The product was filtered through 100 mL of silica gel, eluting a with 15% ethyl acetate/hexanes then 25% ethyl acetate/hexanes to give 0.200 g of the desired product: mp 91-95° C. MS (ES) m/z (relative intensity): 356 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245799B1
Source datasetuspto-grants-2001_06
ORD IDord-5e6e155447f34d639c8d0f88bb7dc6a9
Source noteuspto-grants-2001_06