Sodium → HCID 20260938, compound

HRID 648056Notes

Reaction equation

HRID 648056 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

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

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 3 hours
  3. customevaporated
  4. dissolutionThe residue was dissolved in water
  5. washthe solution was washed several times with ether
  6. customto give a gummy solid which
  7. filtrationwas filtered off
  8. washwashed with water
  9. customdried
  10. customchromatographed on silica gel
  11. washElution with chloroform
  12. customgave some impurity
  13. washfurther elution with chloroform/methanol (9:1)
  14. customgave a solid which
  15. 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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