Hydrogen Bromide → HCID 178515815, compound
Reaction equation
[CH2:1]([C:8]1[C:13]([Br:14])=[CH:12][CH:11]=[C:10]([O:15]C)[N:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br>O>[CH2:1]([C:8]1[C:13]([Br:14])=[CH:12][CH:11]=[C:10]([OH:15])[N:9]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 72.5 g of 2-benzyl-3-bromo-6-methoxypyridine and 300 ml of 47% hydrobromic acid was heated under stirring for 4 hours in an oil bath kept at 100° C. After cooling as it was, 500 ml of water was added thereto. The resulting crystals were collected by filtration, washed with water and diethyl ether, air-dried and then dried under heating under reduced pressure, to give 63.8 g of the target compound.
Workup
- temperaturewas heated
- customkept at 100° C
- temperatureAfter cooling as it
- filtrationThe resulting crystals were collected by filtration
- washwashed with water and diethyl ether
- customair-dried
- customdried
- temperatureunder heating under reduced pressure
Sources & evidence
- ORD record
- ord-f902d7eb8cf7490f9f8ce16adbe57692
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06599917B1
Reaction notes
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