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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091822Generated: November 1, 2026

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

https://huagongshe.com/reaction/1091822

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 numberUS08129399B2
Source datasetuspto-grants-2012_03
ORD IDord-15d1f9e5bfe14db0a1c3e9b64ab323af
Source noteuspto-grants-2012_03