Phosgene → HCID 20406860, compound
Reaction equation
C([O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=O)NN.[C:13]([O:17]CC)(=O)[NH:14][NH2:15].C(Cl)([Cl:22])=O>C(OCC)C>[CH2:6]([O:5][NH:15][NH:14][C:13]([Cl:22])=[O:17])[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Example 1 was repeated but substituting benzyl carbazate (41.5 g, 0.25 mole) for the ethyl carbazate and using phosgene (30 ml, 0.4 mole) in diethyl ether. 2-Benzyloxyhydrazinecarbonyl chloride was isolated as a solid (53 g, 93%) mp 62°-64° C., whose ir spectrum was similar to that of 2-ethoxycarbonylhydrazinecarbonyl chloride.
Sources & evidence
- ORD record
- ord-cc54c943866d4fc393e5d9e0d7b6fccf
- Source dataset
- uspto-grants-1985_02
- Patent number
- US04501860
Reaction notes
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