Ethanol → HCID 12902853, compound

HRID 1680702Notes

Reaction equation

HRID 1680702 reaction equation
[C:1]([C:3]1[C:11]2[O:10][CH:9]=[C:8]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)[C:7]=2[CH:6]=[C:5]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:4]=1)#N.[OH-:24].[K+].C(O)C.[OH2:29]>>[C:12]1([C:8]2[C:7]3[CH:6]=[C:5]([C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)[CH:4]=[C:3]([C:1]([OH:29])=[O:24])[C:11]=3[O:10][CH:9]=2)[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1

Participants

5

Reactant 4

HCID 702EthanolHCID 962WaterHCID 14797Potassium HydroxideHCID 12902852HCID 12902852, compound

Product 1

HCID 12902853HCID 12902853, compound

Procedure

A mixture containing 30 g. (0.10 mole) of the product of step C, 14.5 g. (0.22 mole) of 85 percent potassium hydroxide, 400 ml. of ethanol and 50 ml. of water is heated at its reflux temperature for 16 hours, cooled and filtered. The product is washed with ethanol, suspended in water and acidified with 6 N hydrochloric acid. The mixture is heated on a steam bath for one hour, cooled and filtered. Recrystallization from ethanol provides 3,5-diphenylbenzofuran-7-carboxylic acid as a white solid.

Workup

  1. additionA mixture containing 30 g
  2. temperaturereflux temperature for 16 hours
  3. temperaturecooled
  4. filtrationfiltered
  5. washThe product is washed with ethanol
  6. temperatureThe mixture is heated on a steam bath for one hour
  7. temperaturecooled
  8. filtrationfiltered
  9. customRecrystallization from ethanol

Sources & evidence

ORD record
ord-4fc49d6f7d724e31a5ebc11bef557143
Source dataset
uspto-grants-1981_06
Patent number
US04275221

Reaction notes

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