Boron → HCID 178427663, compound
Reaction equation
[S:1]([C:5]1[CH:11]=[CH:10][C:8]([CH3:9])=[CH:7][CH:6]=1)([OH:4])(=[O:3])=[O:2].[OH:12][NH:13][C:14]([NH:16][NH2:17])=[NH:15].[B]>C(OCC)(OCC)OCC>[S:1]([C:5]1[CH:11]=[CH:10][C:8]([CH3:9])=[CH:7][CH:6]=1)([OH:4])(=[O:3])=[O:2].[OH:12][N:13]=[C:14]1[N:15]=[CH:5][N:17]=[N:16]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of N-hydroxy-N′-aminoguanidine tosylate (0.66 g; 2.5 mMol) in triethyl orthoformate (1.5 mL) in the presence of boron trifuloride etherate (10 mg) was stirred at room temperature during 8 h. The residue was filtered off and the product crystallised from the ethanol.
Workup
- filtrationThe residue was filtered off
- customthe product crystallised from the ethanol
Sources & evidence
- ORD record
- ord-13378f0633194b70835b1aae09a31a83
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06599943B1
Reaction notes
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