Sodium → HCID 20260938, compound
Reaction equation
[Na].C([O:4][C:5](=[O:24])[CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][C:15]2[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=2)=[CH:10][C:9]=1[C:21](=O)[CH3:22])C>C(O)C>[CH3:22][C:21]1[C:9]2[CH:10]=[C:11]([CH2:14][C:15]3[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=3)[CH:12]=[CH:13][C:8]=2[O:7][C:6]=1[C:5]([OH:4])=[O:24]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium (0.50 g.) was dissolved in ethanol (10 ml.) and a solution of 2-acetyl-4-(3-pyridylmethyl)phenoxyacetic acid ethyl ester (4.70 g.) in ethanol (15 ml.) was added. The mixture was heated under reflux for 3 hours and then evaporated. The residue was dissolved in water and the solution was washed several times with ether. The aqueous layer was acidified with glacial acetic acid to give a gummy solid which was filtered off, washed with water, dried and chromatographed on silica gel. Elution with chloroform gave some impurity and then further elution with chloroform/methanol (9:1) gave a solid which was crystallized from ethanol to give 3-methyl-5-(3-pyridylmethyl)benzofuran-2-carboxylic acid (0.75 g.), m.p. 223°-225° C.
Workup
- temperatureThe mixture was heated
- temperatureunder reflux for 3 hours
- customevaporated
- dissolutionThe residue was dissolved in water
- washthe solution was washed several times with ether
- customto give a gummy solid which
- filtrationwas filtered off
- washwashed with water
- customdried
- customchromatographed on silica gel
- washElution with chloroform
- customgave some impurity
- washfurther elution with chloroform/methanol (9:1)
- customgave a solid which
- customwas crystallized from ethanol
Sources & evidence
- ORD record
- ord-a2dce427facf46e38a747764c24ab742
- Source dataset
- uspto-grants-1983_10
- Patent number
- US04410539
Reaction notes
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