Hydrochloric Acid → (2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-yl)hydrazine
Reaction equation
Cl.[CH3:2][C:3]1([CH3:18])[CH2:7][C:6]2[CH:8]=[CH:9][CH:10]=[C:11]([N:12](S(O)(=O)=O)[NH2:13])[C:5]=2[O:4]1>C(O)C>[CH3:2][C:3]1([CH3:18])[CH2:7][C:6]2[CH:8]=[CH:9][CH:10]=[C:11]([NH:12][NH2:13])[C:5]=2[O:4]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
18 g of hydrogen chloride was introduced into a stirred slurry of 56 g of (1B) in 250 ml of ethanol. The resulting mixture was stirred for 3 hours, and the solvent was evaporated. The residue was dissolved in 50 ml of water, the solution was made basic with aqueous sodium hydroxide, and extracted with ether. The extract was washed with cold water, dried (MgSO4), and filtered, and the solvent was evaporated to give 2,3-dihydro-2,2-dimethyl-7-hydrazinobenzofuran (1C) as a dark oil.
Workup
- customthe solvent was evaporated
- dissolutionThe residue was dissolved in 50 ml of water
- extractionextracted with ether
- washThe extract was washed with cold water
- dry with materialdried (MgSO4)
- filtrationfiltered
- customthe solvent was evaporated
Sources & evidence
- ORD record
- ord-adf922d6af9f4144bca41ce4c1158250
- Source dataset
- uspto-grants-1983_09
- Patent number
- US04406910
Reaction notes
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