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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Dichloromethane ethylacetate | HCID 21226138 | — |
| Reactant | 5-Benzyloxy-2-difluoromethyl-pyran-4-one | HCID 59818292 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Benzyloxy-2-difluoromethyl-1H-pyridin-4-one | HCID 67282165 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026261B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-888f2b8436ea4022866f489cd13cff63 |
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| Source note | uspto-grants-2011_09 |
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