Sodium ethanethiolate → HCID 53892591, compound
Reaction equation
C[O:2][C:3]1[CH:30]=[CH:29][C:6]([C:7]([C:9]2[O:10][C:11]3[C:16]([C:17](=[N:19][S:20]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)(=[O:22])=[O:21])[CH:18]=2)=[CH:15][CH:14]=[CH:13][CH:12]=3)=[O:8])=[CH:5][CH:4]=1.[S-]CC.[Na+]>CN(C)C=O.O.ClCCl>[OH:2][C:3]1[CH:4]=[CH:5][C:6]([C:7]([C:9]2[O:10][C:11]3[C:16]([C:17](=[N:19][S:20]([C:23]4[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=4)(=[O:22])=[O:21])[CH:18]=2)=[CH:15][CH:14]=[CH:13][CH:12]=3)=[O:8])=[CH:29][CH:30]=1Participants
6
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
Combine 2-(4-methoxybenzoyl)-4-benzenesulfonylimino-4H-chromene (1 mmol) and sodium thioethoxide (2 mmol) in dimethylformamide (5 mL). Stir for 48 hours. Dilute the reaction mixture with water and dichloromethane. Separate the organic layer, dry over MgSO4, filter, and evaporate in vacuo. Chromatograph on silica gel to give the title compound.
Workup
- customSeparate the organic layer
- dry with materialdry over MgSO4
- filtrationfilter
- customevaporate in vacuo
Sources & evidence
- ORD record
- ord-7de88091c92744358dfa2352aa4edfc6
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05684017
Reaction notes
Loading…