Hydrazine hydrate (1:1) → 3-Amino-1-(3,5-difluorophenyl)urea
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([NH:9][C:10](=[O:18])OC2C=CC=CC=2)[CH:5]=[C:6]([F:8])[CH:7]=1.O.[NH2:20][NH2:21]>>[F:1][C:2]1[CH:3]=[C:4]([NH:9][C:10](=[O:18])[NH:20][NH2:21])[CH:5]=[C:6]([F:8])[CH:7]=1Participants
3
Procedure
To a solid 100 mg of O-phenyl 3,5-difluorophenylcarbamate 0.7 mL of hydrazine monohydrate was added. After stirring for 3 h at room temperature a white solid is collected by filtration, washed with water and ether. Removal of traces of the solvents in vacuo gives 4-(3,5-difluorophenyl)-semicarbazide: m.p. 177°-179° C.
Workup
- filtrationis collected by filtration
- washwashed with water and ether
- customRemoval of traces of the solvents in vacuo
Sources & evidence
- ORD record
- ord-1c2a9e154d884b018656e8f52aecdcc5
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05098466
Reaction notes
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