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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187456Generated: November 2, 2026

5-Benzyloxy-2-difluoromethyl-1-ethyl-1H-pyridin-4-one → 2-Difluoromethyl-1-ethyl-5-hydroxy-1H-pyridin-4-one

https://huagongshe.com/reaction/1187456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzyloxy-2-difluoromethyl-1-ethyl-1H-pyridin-4-oneHCID 67282967—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-Difluoromethyl-1-ethyl-5-hydroxy-1H-pyridin-4-oneHCID 2501890564.2%

Reaction Steps

A mixture of 5-benzyloxy-2-difluoromethyl-1-ethyl-1H-pyridin-4-one (2.00 g, 7.16 mmol) and 10% Pd/C (200 mg) in methanol (75 mL) was hydrogenated under 15.0 psi pressure in a hydrogen atmosphere in a Parr apparatus for 23 min. The reaction mixture was worked up as described above. The title compound (0.87 g, 64%) was obtained as an off-white solid. HPLC purity (peak area percent) of the compound is 97.7% at λ=280 nm using HPLC Method 1 as described above. 1H NMR (400 MHz, DMSO-D6) δ (ppm): 7.61 (s, 1H), 7.15 (t, J=52.7 Hz, 1H, CF2H), 6.46 (s, 1H), 4.03 (q, J=7.0 Hz, 2H, N—CH2), 1.31 (t, J=7.1 Hz, 3H, CH3); MS-ESI (m/z): 190.2 [M+1]+, 142.2 (100%); Anal. Calcd. for C8H9F2NO2: C, 50.80; H, 4.80; N, 7.40%. Found: C, 50.64; H, 4.85; N, 7.38%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673943B2
Source datasetuspto-grants-2014_03
ORD IDord-b76fd85559384e8c973f8d3603101aca
Source noteuspto-grants-2014_03