L-Tartaric acid → HCID 86748375, compound
Reaction equation
[C:1]([OH:10])(=[O:9])[C@@H:2]([C@H:4]([C:6]([OH:8])=[O:7])[OH:5])[OH:3]>O>[OH2:3].[OH2:3].[OH2:3].[C:6]([CH:4]([CH:2]([C:1]([OH:10])=[O:9])[OH:3])[OH:5])([OH:8])=[O:7].[C:6]([CH:4]([CH:2]([C:1]([OH:10])=[O:9])[OH:3])[OH:5])([OH:8])=[O:7]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of the protected compound obtained according to Example 38 (0.26 g, 0.5 mmol) and L(+)-tartaric acid (0.23 g, 1.5 mmol) in water (2.5 ml) was heated under reflux for one hour and allowed to cool to room temperature. The separated precipitate was collected to give the ditartrate-trihydrate of the title compound which was identical with the salt obtained according to Method A) above, yield: 65.8%, mp 169°-175° C.
Workup
- additionA mixture of the protected compound
- customobtained
- temperaturewas heated
- temperatureunder reflux for one hour
- customThe separated precipitate was collected
Sources & evidence
- ORD record
- ord-7164aee1d9a742fab7177d5c7043c5a3
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05380724
Reaction notes
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