Sodium Hydroxide → HCID 15225070, compound
Reaction equation
[CH3:1][N:2]([CH3:16])[C:3]1([C:12](OC)=[O:13])[C:8]2[CH:9]=[CH:10][S:11][C:7]=2[CH2:6][CH2:5][CH2:4]1.[H-].[Li+].[Al+3].[H-].[H-].[H-].[OH-].[Na+]>CCOCC>[CH3:1][N:2]([CH3:16])[C:3]1([CH2:12][OH:13])[C:8]2[CH:9]=[CH:10][S:11][C:7]=2[CH2:6][CH2:5][CH2:4]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
65 ml of ether solution containing 7.77 g of 4-dimethylamino-4-methoxycarbonyl-4,5,6,7-tetrahydro-1-benzothiophene obtained in Step 2 was added to an ice-cooled suspension of aluminum lithium hydride (1.23 g) in ether, then stirred for 20 minutes at room temperature. The reaction mixture was added with 5% NaOH solution, filtrated to remove the insoluble matters, followed by drying the organic phase.
Workup
- temperaturecooled
- filtrationfiltrated
- customto remove the insoluble matters
- customby drying the organic phase
Sources & evidence
- ORD record
- ord-05bc694dc2dd46c3915f6150d0507aac
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05380748
Reaction notes
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