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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474006Generated: November 3, 2026

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

https://huagongshe.com/reaction/474006

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 was 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 numberUS08637511B2
Source datasetuspto-grants-2014_01
ORD IDord-96386d14b5924ccebf854807cfa45d6f
Source noteuspto-grants-2014_01