Hydrazine hydrate (1:1) → HCID 23362742, compound
Reaction equation
Cl[C:2](=[N:11][N:12]=[C:13](Cl)[C:14]1[C:19]([F:20])=[CH:18][CH:17]=[CH:16][C:15]=1[F:21])[C:3]1[C:8]([F:9])=[CH:7][CH:6]=[CH:5][C:4]=1[F:10].O.[NH2:24][NH2:25]>O1CCCC1>[F:10][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]([F:9])[C:3]=1[C:2]1[N:24]=[N:25][C:13]([C:14]2[C:19]([F:20])=[CH:18][CH:17]=[CH:16][C:15]=2[F:21])=[N:12][N:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 0.9 g of bis[chloro-(2,6-difluorobenzylidene)]hydrazine [prepared in the preceding step b.)] in 18 ml of tetrahydrofuran of 40° C. temperature, 0.59 ml of hydrazine hydrate is dropped over 1 minute. After filtering the precipitate is washed with water and dried to give 0.5 g of desired product as yellow crystals. The melting point is 225.5° C.
Workup
- filtrationAfter filtering the precipitate
- washis washed with water
- customdried
Sources & evidence
- ORD record
- ord-cf9c58307973414a9c1b040595f9fdab
- Source dataset
- uspto-grants-1996_12
- Patent number
- US05587370
Reaction notes
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