HCID 54158441, compound → HCID 54416739, compound
Reaction equation
[OH:1][C:2]([P:18](=[O:21])([OH:20])[OH:19])([P:14](=[O:17])([OH:16])[OH:15])[CH2:3][CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH:5]1[S:10]C(=O)C>Cl.O>[OH:1][C:2]([P:14](=[O:15])([OH:16])[OH:17])([P:18](=[O:19])([OH:20])[OH:21])[CH2:3][CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH:5]1[SH:10]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
[1-Hydroxy-2-(2-(acetylthio)cyclohexyl)ethylidene]bis[phosphonic acid] is heated at reflux in concentrated hydrochloric acid for 7 hours. The reaction is concentrated under reduced pressure and the solid residue is triturated in ethanol. The product is obtained by recrystallization the crude solid in ethanol and water.
Workup
- concentrationThe reaction is concentrated under reduced pressure
- customthe solid residue is triturated in ethanol
- customThe product is obtained by recrystallization the crude solid in ethanol
Sources & evidence
- ORD record
- ord-a87cb3130d934237aad5fdd6538aa0ad
- Source dataset
- uspto-grants-1998_10
- Patent number
- US05824661
Reaction notes
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