5,6,7,8-Tetrahydro-4-methyl-8-(phenylsulphinyl)quinoline → 4-Methyl-5,6-dihydroquinoline
Reaction equation
[CH3:1][C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH:7](S(C3C=CC=CC=3)=O)[C:6]=2[N:5]=[CH:4][CH:3]=1>C1(C)C=CC=CC=1>[CH3:1][C:2]1[C:11]2[CH2:10][CH2:9][CH:8]=[CH:7][C:6]=2[N:5]=[CH:4][CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The crude product of Step 5 (10.8 g, 40.0 mmol) was heated under reflux in toluene (100 m) for 30 min, cooled to room temperature, and extracted with 1N-HCl (3×50 ml). The extracts were basified with 10N-NaOH and extracted with dichloromethane (3×200 ml). The organic extracts were dried (MgSO4) and evaporated in vacuo to give an oil which was purified by chromatography (alumina; ether) to give the product (5.5 g, 95%) as an oil.
Workup
- extractionextracted with 1N-HCl (3×50 ml)
- extractionextracted with dichloromethane (3×200 ml)
- dry with materialThe organic extracts were dried (MgSO4)
- customevaporated in vacuo
- customto give an oil which
- customwas purified by chromatography (alumina; ether)
Sources & evidence
- ORD record
- ord-0d0ed2b5e5f24819bcc73916a78afeb0
- Source dataset
- uspto-grants-1993_03
- Patent number
- US05194439
Reaction notes
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