Ethanol → HCID 86737317, compound
Reaction equation
[Cl:1][C:2]([CH:5]1[O:10][CH2:9][C:8]2[CH:11]=[CH:12][CH:13]=[CH:14][C:7]=2[O:6]1)([Cl:4])[Cl:3].O.[NH2:16][NH2:17].[CH2:18](O)[CH3:19]>>[C:18](=[N:16][NH2:17])([C:12]1[CH:13]=[CH:14][C:7]2[O:6][CH:5]([C:2]([Cl:1])([Cl:4])[Cl:3])[O:10][CH:9]([C:2]([Cl:4])([Cl:3])[Cl:1])[C:8]=2[CH:11]=1)[CH3:19]Participants
4
Procedure
A mixture of 6-acetyl-2,4-bis(trichloromethylbenzo[1,3]dioxin (2.0 g.) and 100% hydrazine hydrate (0.25 g.) in absolute ethanol (25 ml.) was heated under reflux for 16 hours, and cooled to give 6-acetyl-2,4-bis(trichloromethyl)benzo[1,3]dioxin hydrazone, m.p. 159° C.
Workup
- temperaturewas heated
- temperatureunder reflux for 16 hours
- temperaturecooled
Sources & evidence
- ORD record
- ord-718d4b98a81f44c7aa217a7b4f3e1d28
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04232032
Reaction notes
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