Carbon tetrabromide → 5-(Bromomethyl)-2,3-dichloropyridine
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9]O)[CH:5]=[N:6][C:7]=1[Cl:8].C(Br)(Br)(Br)[Br:12].C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>ClCCl>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][Br:12])[CH:5]=[N:6][C:7]=1[Cl:8]Participants
5
Procedure
5,6-dichloro-3-pyridinemethanol (1.0 eq.) was taken up in dichloromethane and stirred overnight with carbon tetrabromide (1.5 eq.) and 1,3-bis(diphenylphosphino)propane (0.75 eq.) Ether was added to the solution and filtration followed by concentration of the filtrate afforded the 5,6-dichloro-3-bromomethylpyridine in 130% yield.
Workup
- additionwas added to the solution and filtration
Sources & evidence
- ORD record
- ord-8a14207742734dabb64060f99264568b
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07906548B2
Reaction notes
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