5-Nitrofurfural → HCID 18921656, compound
Reaction equation
Cl.[CH3:2][N:3]([CH3:7])[CH2:4][CH2:5][SH:6].[H-].[Na+].[N+]([C:13]1[O:17][C:16]([CH:18]=[O:19])=[CH:15][CH:14]=1)([O-])=O>CS(C)=O>[CH3:2][N:3]([CH3:7])[CH2:4][CH2:5][S:6][C:13]1[O:17][C:16]([CH:18]=[O:19])=[CH:15][CH:14]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2-Dimethylaminoethanethiol hydrochloride was suspended in dry DMSO and sodium hydride was added. The reaction mixture was left stirring for 40 minutes before 5-nitro-2-furancarboxaldehyde was added. The reaction mixture was allowed to stir for 30 minutes at room temperature, to give the title compound. This is the starting aldehyde used in the synthesis of compound 5253.
Workup
- waitThe reaction mixture was left
- additionwas added
Sources & evidence
- ORD record
- ord-7863ee0f3ae542d48883e35032e826bf
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05750530
Reaction notes
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