Carbon tetrabromide → 2-(1-Bromopropyl)-6-chloropyridine
Reaction equation
[Cl:1][C:2]1[N:7]=[C:6]([CH:8](O)[CH2:9][CH3:10])[CH:5]=[CH:4][CH:3]=1.C(Br)(Br)(Br)[Br:13].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C1COCC1>[Br:13][CH:8]([C:6]1[CH:5]=[CH:4][CH:3]=[C:2]([Cl:1])[N:7]=1)[CH2:9][CH3:10]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 1-(6-chloropyridin-2-yl)propan-1-ol (0.497 g, 2.90 mmol), CBr4 (1.2 g, 3.62 mmol) and triphenylphosphine (0.987 g, 3.76 mmol) in 25 mL of THF was stirred at room temperature for 2 h. The solid was filtered off and washed with THF. The filtrate was concentrated and residue was purified by chromatography on silica gel, eluting with 10 to 50% EtOAc/hexane to provide the title compound. Mass Spectrum (ESI) m/z=236 (M+1).
Workup
- filtrationThe solid was filtered off
- washwashed with THF
- concentrationThe filtrate was concentrated
- customresidue was purified by chromatography on silica gel
- washeluting with 10 to 50% EtOAc/hexane
Sources & evidence
- ORD record
- ord-8ea63e3f09a448928b79e46efb38be85
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09296736B2
Reaction notes
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