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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772840Generated: November 1, 2026

1,1-Dimethylethyl 3-(difluoromethyl)-4-(phenylmethyl)-1-piperazinecarboxylate → tert-butyl 3-(difluoromethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1772840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Dimethylethyl 3-(difluoromethyl)-4-(phenylmethyl)-1-piperazinecarboxylateHCID 67054946—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Producttert-butyl 3-(difluoromethyl)piperazine-1-carboxylateHCID 6705490697.1%

Reaction Steps

10% Palladium on carbon (65 mg, 0.061 mmol) was added to a solution of tert-butyl 4-benzyl-3-(difluoromethyl)piperazine-1-carboxylate (0.20 g, 0.61 mmol, racemic from Step 3) in methanol (15 mL). The suspension was stirred under an atmosphere of hydrogen provided by a balloon. When the reaction showed no progress, 20% Pd(OH)2 on charcoal (47 mg, 0.061 mmol) was added and the suspension was shaken under 50-55 psi hydrogen for 2 h. The mixture was filtered and solvent removed in vacuo to afford product as a viscous oil (140 mg, 97%). 1H NMR (300 MHz, CDCl3): δ 5.90 (td, 0.1H), 5.52-5.12 (br s, 2H), 4.25-3.96 (br s, 1H), 3.94 (d, 1H), 3.27-2.77 (m, 4H), 1.45 (s, 9H); LCMS (M-tBu+2H)+: 181.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249145B2
Source datasetuspto-grants-2016_02
ORD IDord-f17f880a1b654bfd8f6dff5d2b553259
Source noteuspto-grants-2016_02