Hydrogen Bromide → 4-(bromomethyl)pyridin-2(1H)-one
Reaction equation
[BrH:1].O[CH2:3][C:4]1[CH:9]=[CH:8][NH:7][C:6](=[O:10])[CH:5]=1>>[Br:1][CH2:3][C:4]1[CH:9]=[CH:8][NH:7][C:6](=[O:10])[CH:5]=1Participants
3
Conditions
- Temperature
- 110 °C
Procedure
Hydrobromic acid (2 mL) was added to a solution of 4-(hydroxymethyl)pyridin-2(1H)-one (200 mg, 1.6 mmol) was at 0° C. The mixture was stirred at 110° C. for 3 hours. After cooling to room temperature, the mixture was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (EtOAc/MeOH) to afford the 4-(bromomethyl)pyridin-2(1H)-one. MS ESI calc'd. for C6H7BrNO [M+H]+ 188 and 190. found 188 and 190. 1H NMR (400 MHz, DMSO-d6) δ 11.55 (s, 1H), 7.36 (d, J=6.8 Hz, 1H), 6.39 (s, 1H), 6.17 (d, J=6.8 Hz, 1H), 4.45 (s, 2H).
Workup
- customwas at 0° C
- temperatureAfter cooling to room temperature
- concentrationthe mixture was concentrated under reduced pressure
- customThe residue was purified by column chromatography on silica gel (EtOAc/MeOH)
Sources & evidence
- ORD record
- ord-b7137d735aac4ebcba645e4246269e40
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09242984B2
Reaction notes
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