Reaction equation
[CH2:1]([N:8]1[CH2:13][CH2:12][C:11](O)([C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(OS([O-])(=O)=O)([O-])(=O)=O.[K+].[K+]>C1C2C(CCCC2)CCC1.O>[CH2:1]([N:8]1[CH2:9][CH:10]=[C:11]([C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)[CH2:12][CH2:13]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A dispersion of 4.52 g (16.8 mmol) of 1'-benzyl-2',3',5',6'-tetrahydro-1'H-[3,4']bipyridinyl-4'-ol and 18 g (71 mmol) of potassium disulphate in 35 ml of decalin was stirred at 190° C. for 30 minutes. After cooling to room temperature the reaction mixure was dissolved in water and extracted twice with 50 ml of toluene each time. Subsequently, the aqueous phase was made alkaline with sodium hydroxide solution and extracted with ethyl acetate. The ethyl acetate phase was thereafter dried over sodium sulphate and evaporated under reduced pressure. For purification, the crude product was chromatographed on silica gel using a 98:2:0.1 mixture of methylene chloride, methanol and ammonia as the eluent. There were obtained 4.03 g (61% of theory) of 1'-benzyl-1',2',3',6'-tetrahydro-3,4'-bipyridine as a yellowish oil; MS: 250 (M)+.
Workup
- extractionextracted twice with 50 ml of toluene each time
- extractionextracted with ethyl acetate
- dry with materialThe ethyl acetate phase was thereafter dried over sodium sulphate
- customevaporated under reduced pressure
- customFor purification
- customthe crude product was chromatographed on silica gel using
- additiona 98:2:0.1 mixture of methylene chloride, methanol and ammonia as the eluent
Sources & evidence
- ORD record
- ord-96ec8ca9c6bc4421be6ee1a9f27c6497
- Source dataset
- uspto-grants-2000_04
- Patent number
- US06051712
Linked notes
Loading…