Benzylhydrazine dihydrochloride → HCID 2806526, compound
Reaction equation
Br[CH:2](Br)[C:3]1[C:4]([C:9]([OH:11])=O)=[CH:5][CH:6]=[CH:7][CH:8]=1.Cl.Cl.[CH2:15]([NH:22][NH2:23])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(N(CC)CC)C>[CH2:15]([N:22]1[N:23]=[CH:2][C:3]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:9]1=[O:11])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
α,α-dibromo-o-toluic acid (29.4 g), benzylhydrazine dihydrochloride (19.5 g) and triethylamine (60 g) were allowed to react as in Example 4. There was obtained 12.1 g (yield: 51%) of 2-benzyl-1-phthalazinone having a melting point of 104°-105° C.
Sources & evidence
- ORD record
- ord-b75573a33744473db85f48a17fe97cf9
- Source dataset
- uspto-grants-1978_06
- Patent number
- US04096143
Reaction notes
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