Hydrochloric Acid → HCID 67166220, compound
Reaction equation
C([O:3][C:4]([C:6]1[O:7][C:8]([N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)=[CH:9][C:10]=1[CH3:11])=[O:5])C.[OH-].[Na+].Cl>C(O)C>[N:12]1([C:8]2[O:7][C:6]([C:4]([OH:5])=[O:3])=[C:10]([CH3:11])[CH:9]=2)[CH2:16][CH2:15][CH2:14][CH2:13]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The 5-pyrrolidine-1-yl-methyl-furan-2-carboxylic acid ethyl ester (770 mg, 3.45 mmol) obtained in Example 55 (1) was dissolved in ethanol (4 ml). A 1 N sodium hydroxide aqueous solution (5.17 ml) was added dropwise to the solution, and the mixture was stirred overnight. The reaction mixture was neutralized with a 1 N hydrochloric acid solution (5.17 ml), and then ethanol was evaporated. The residue was dried to afford 5-pyrrolidine-1-yl-methyl-furan-2-carboxylic acid containing sodium chloride (1.08 g, sodium chloride content: 38% wt., quant.) as a white solid, which was used directly for the following reaction.
Workup
- customethanol was evaporated
- customThe residue was dried
Sources & evidence
- ORD record
- ord-0880040c7f0b4ee2b78491ee96b2d59d
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07951956B2
Reaction notes
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