Hydrazinecarboxaldehyde → HCID 178513097, compound
Reaction equation
[CH:1]([NH:3][NH2:4])=[O:2].[Cl:5][C:6]([Cl:12])([Cl:11])[C:7](=[NH:10])OC>>[Cl:5][C:6]([Cl:12])([Cl:11])[C:7]([NH:4][NH:3][CH:1]=[O:2])=[NH:10]Participants
3
Procedure
A mixture of 4.2 g (0.07 mole) formylhydrazine and 20 ml (28.5 g, 0.16 mole) methyl 2,2,2-trichloroacetimidate was stirred at room temperature. After 10 minutes a vigorous reaction occurred and the temperature rose to 65° C. The beige solid that formed was washed with petroleum ether and dried to give 11.0 g [77%, mp 124°-126° C. (decomposed)] of product. An analytical sample was recrystallized from toluene [mp 128°-130° C. (decomposed)]. The structure was confirmed via infrared and elemental analysis.
Workup
- customAfter 10 minutes a vigorous reaction
- customrose to 65° C
- customThe beige solid that formed
- washwas washed with petroleum ether
- customdried
- customto give 11.0 g [77%, mp 124°-126° C. (decomposed)] of product
- customAn analytical sample was recrystallized from toluene [mp 128°-130° C. (decomposed)]
Sources & evidence
- ORD record
- ord-cc53b38cab1140f582f14f7c5a114153
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04282169
Reaction notes
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