Bromine → HCID 58110166, compound
Reaction equation
[Br:1]Br.[CH2:3]([CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][C:11]1=[O:16])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>C(Cl)(Cl)Cl>[CH2:3]([CH:10]1[CH2:15][CH2:14][CH2:13][CH:12]([Br:1])[C:11]1=[O:16])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Step AAD (1): Followed the method of B. Miller and H.-S. Wong Tetrahedron 1972, 28, 2369. Bromine (0.082 mL, 1.59 mmol) in was added dropwise over a period of 15 min to a solution of 2-benzylcyclohexanone (300 mg, 1.593 mmol) in chloroform (5 mL). The reaction mixture was stirred at rt for 2 h, then concentrated in vacuo to afford 2-benzyl-6-bromocyclohexanone. The crude product, which is prone to decomposition, was used for subsequent chemistry without purification or characterization.
Workup
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-41ef70b537094fd480e3e0b782bc9d01
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08349880B2
Reaction notes
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