2-Furancarbonyl chloride → HCID 12747893, compound

HRID 261029Notes

Reaction equation

HRID 261029 reaction equation
[Cl:1][C:2]1[CH:13]=[CH:12][C:5]2[CH2:6][CH:7]([C:9]([OH:11])=[O:10])[O:8][C:4]=2[C:3]=1[Cl:14].[O:15]1[CH:19]=[CH:18][CH:17]=[C:16]1[C:20](Cl)=[O:21].[Cl-].[Al+3].[Cl-].[Cl-]>C(Cl)Cl>[Cl:1][C:2]1[C:13]([C:20]([C:16]2[O:15][CH:19]=[CH:18][CH:17]=2)=[O:21])=[CH:12][C:5]2[CH2:6][CH:7]([C:9]([OH:11])=[O:10])[O:8][C:4]=2[C:3]=1[Cl:14]

Participants

5

Reactant 3

HCID 682422-Furancarbonyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 98160656,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic Acid

Product 1

HCID 12747893HCID 12747893, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a well stirred mixture of 6,7-dichloro-2,3-dihydro-benzofuran-2-carboxylic acid (3.3 g.), furan-2-carbonyl-chloride (3.6 g.) and 200 ml methylene chloride, protected from the atmosphere with a calcium chloride tube is added anhydrous aluminum chloride (3.7 g.) over an one-half hour period. The reaction solution is stirred 18 hours at 25° C. and then refluxed for 1 hour. The solvent is removed and the residue added to ice water (200 ml.) and hydrochloric acid (20 ml.). The product is extracted into ether, washed with water, then extracted into aqueous sodium bicarbonate (200 ml.) from which the sodium salt of the product precipitates. The sodium salt of the product is placed in a separatary funnel with dilute hydrochloric acid (100 ml.) and ether (100 ml.) and shaken until the solid dissolves. The ether solution is washed with water, brine, dried over magnesium sulfate and the ether distilled at reduced pressure. The 6,7-dichloro-2,3-dihydro-5-(2-furoyl) benzofuran-2-carboxylic acid melts at 166° C. after crystallization from acetonitrile/n-butyl chloride.

Workup

  1. customprotected from the atmosphere with a calcium chloride tube
  2. stirringThe reaction solution is stirred 18 hours at 25° C.
  3. temperaturerefluxed for 1 hour
  4. customThe solvent is removed
  5. additionthe residue added to ice water (200 ml.) and hydrochloric acid (20 ml.)
  6. extractionThe product is extracted into ether
  7. washwashed with water
  8. extractionextracted into aqueous sodium bicarbonate (200 ml.) from which the sodium salt of the product
  9. customprecipitates
  10. customThe sodium salt of the product is placed in a separatary funnel with dilute hydrochloric acid (100 ml.) and ether (100 ml.)
  11. stirringshaken until the solid
  12. dissolutiondissolves
  13. washThe ether solution is washed with water, brine
  14. dry with materialdried over magnesium sulfate
  15. distillationthe ether distilled at reduced pressure
  16. customThe 6,7-dichloro-2,3-dihydro-5-(2-furoyl) benzofuran-2-carboxylic acid melts at 166° C. after crystallization from acetonitrile/n-butyl chloride

Sources & evidence

ORD record
ord-bc64fcf4b70845529c0bb2ff71963c6d
Source dataset
uspto-grants-1979_08
Patent number
US04163794

Reaction notes

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