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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013116Generated: November 1, 2026

1-(Diphenylmethyl)-3-phenylazetidine → 3-Phenylazetidine

https://huagongshe.com/reaction/1013116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Diphenylmethyl)-3-phenylazetidineHCID 16089447—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product3-PhenylazetidineHCID 2890158634%

Reaction Steps

Add 20% palladium hydroxide on activated carbon (0.130 g) and ethanol (25 mL) to a Parr pressure vessel. Purge the reaction vessel with nitrogen, pressurize the reaction mixture with hydrogen (400 kPa), seal the vessel and agitate the mixture at RT for 15 min. Vent the hydrogen from the reaction vessel and purge the reaction vessel with nitrogen. Add 1-benzhydryl-3-phenylazetidine (0.515 g, 0.00172 mol) and ethanol (75 mL) to the pressure vessel. Purge the reaction vessel with nitrogen, pressurize the reaction mixture with hydrogen (400 kPa), seal the vessel and agitate the reaction at RT for 20 h. Turn off the agitation, vent the excess hydrogen from the vessel, purge the vessel with nitrogen and filter the reaction mixture to remove the palladium on carbon catalyst. Concentrate and purify (silica gel chromatography, eluting with 5:95 to 10:90 2 M ammonia in methanol:DCM) to give the title compound (76 mg, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981882B2
Source datasetuspto-grants-2011_07
ORD IDord-79662dc2a31f404cb9b2129b40f3d664
Source noteuspto-grants-2011_07