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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490243Generated: October 28, 2026

1-Benzhydryl-3-cyclopropyl-3-fluoroazetidine hydrochloride → 3-Cyclopropyl-3-fluoroazetidine hydrochloride

https://huagongshe.com/reaction/490243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzhydryl-3-cyclopropyl-3-fluoroazetidine hydrochlorideHCID 66589518—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-Cyclopropyl-3-fluoroazetidine hydrochlorideHCID 6658964293.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To wet 10% palladium on carbon (Degussa catalyst) under nitrogen was added ethanol (100 ml). A solution of 1-Benzhydryl-3-cyclopropyl-3-fluoroazetidine hydrochloride (6.74 g, 21.23 mmol) in ethanol (50 ml) was added to the catalyst and the mixture hydrogenated at 60 psi on the Parr shaker hydrogenation apparatus for 5 hrs. The reaction was filtered through celite and concentrated to an oil. Ether (50 ml) was added and the mixture cooled to 0° C. and stirred until a precipitate formed. The suspension was filtered and the filter cake washed with ether (20 ml) and the solid dried under vacuum. This furnished the product as an off white solid (3.00 g, 93%). 1H NMR d6-DMSO δ 0.52-0.56 (2H, m), 0.59-0.64 (2H, m), 1.35-1.40 (1H, m), 3.91-4.10 (4H, m), 4.01-4.23 (4H, m), 9.50 (1H, brs), 9.63 (1H, brs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528142B2
Source datasetuspto-grants-2009_05
ORD IDord-3ec0a7b2f59043d8b750fd6ae6c021c6
Source noteuspto-grants-2009_05