Hydrazine → HCID 15730198, compound
Reaction equation
[OH:1][C:2]1[C:11]([OH:12])=[CH:10][C:9]([S:13]([OH:16])(=[O:15])=[O:14])=[CH:8][C:3]=1[C:4](OC)=[O:5].[K].[NH2:18][NH2:19]>CO>[OH:1][C:2]1[C:11]([OH:12])=[CH:10][C:9]([S:13]([OH:16])(=[O:15])=[O:14])=[CH:8][C:3]=1[C:4]([NH:18][NH2:19])=[O:5]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2,3-Dihydroxy-5-sulfobenzoic acid, methyl ester, monopotassium salt (2.7 g, 9.4 mmole) and neat hydrazine (0.88 ml, 28 mmoles) in 100 ml of methanol were refluxed for 48 hours. The resulting white precipitate was filtered, dried, and dissolved in water (10 ml). Acidification to pH =2.5 with 2N hydrochloric acid, filtering and drying gave 940 mg of the title compound as a solid.
Workup
- filtrationThe resulting white precipitate was filtered
- customdried
- dissolutiondissolved in water (10 ml)
- filtrationfiltering
- customdrying
Sources & evidence
- ORD record
- ord-1d8af70b0b6e4ccfbc1ea3a5ccd4c863
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05077432
Reaction notes
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