Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913001Generated: November 3, 2026

Ammonium Hydroxide → 5-Benzyloxy-2-difluoromethyl-1H-pyridin-4-one

https://huagongshe.com/reaction/913001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantDichloromethane ethylacetateHCID 21226138—
Reactant5-Benzyloxy-2-difluoromethyl-pyran-4-oneHCID 59818292—
SolventEthanolHCID 702—
Product5-Benzyloxy-2-difluoromethyl-1H-pyridin-4-oneHCID 6728216574%

Reaction Steps

5-Benzyloxy-2-difluoromethyl-pyran-4-one (0.47 g, 1.9 mmol) was dissolved in ethanol (15 mL) to give a slightly yellow clear solution. Ammonium hydroxide (28-30% aqueous solution, 15 mL, 235 mmol) was added at room temperature. The resulting solution was stirred at ambient temperature for 24 hours. The progress of the reaction was monitored by TLC (CH2Cl2/EtOAc, 7/3, v/v) and HPLC Method 2. Volatiles were removed in vacuo and the residue was purified by column chromatography on silica (95/5 then 85/15 CH2Cl2/MeOH, v/v) to give the title compound as a light yellow solid (0.35 g, 74%) with a HPLC purity (peak percent area) of 98.2%. 1H NMR (300 MHz, DMSO-D6) δ (ppm): 10.99 (br. s, 1H), 8.22 (s, 1H), 7.32-7.32 (m, 5H), 7.06 (s, 1H), 6.75 (t, J=55.4 Hz, 1H), 5.23 (s, 2H); MS (m/z) 252 [M+1]+, 192.2, 91.3 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026261B2
Source datasetuspto-grants-2011_09
ORD IDord-888f2b8436ea4022866f489cd13cff63
Source noteuspto-grants-2011_09