Oxalic Acid → HCID 15480258, compound
Reaction equation
[NH2:1][C:2]1([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:7][CH2:6][CH:5]2[CH:3]1[CH:4]2[C:8]([O:10][CH2:11][CH3:12])=[O:9].C(O)(=O)[C:19](O)=[O:20]>C(OCC)(=O)C.C(O)C>[OH-:9].[NH4+:1].[CH3:19][OH:20].[NH2:1][C:2]1([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:7][CH2:6][CH:5]2[CH:3]1[CH:4]2[C:8]([O:10][CH2:11][CH3:12])=[O:9]Participants
Reactant 2
Product 2
Reagents, catalysts & solvents 2
Procedure
A solution of the compounds prepared as described in Example 2 (20.71 g) in ethyl acetate (200 mL) was treated with a solution of oxalic acid (15.46 g) in ethanol (50 mL). The resulting mixture was stirred at room temperature. After one hour, the reaction mixture was treated with additional ethanol (50 mL). After 18 hours, the mixture was filtered, and the filtrate was evaporated to dryness in vacuo. The residue was treated with 1N sodium hydroxide, and the resulting mixture extracted with diethyl ether. The combined ether extracts were washed with brine, dried over potassium carbonate, filtered, and concentrated in vacuo. The residue was purified by silica-gel chromatography, eluting with methylene chloride:5% ammonium hydroxide/methanol (97:3), to give 15.41 g of the title compound.
Workup
- customA solution of the compounds prepared
- waitAfter 18 hours
- filtrationthe mixture was filtered
- customthe filtrate was evaporated to dryness in vacuo
- additionThe residue was treated with 1N sodium hydroxide
- extractionthe resulting mixture extracted with diethyl ether
- washThe combined ether extracts were washed with brine
- dry with materialdried over potassium carbonate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified by silica-gel chromatography
- washeluting with methylene chloride
Sources & evidence
- ORD record
- ord-55462a331faf486395eb0f79f4066ca3
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05750566
Reaction notes
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