Water → 3-Methoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxylic acid

HRID 1982411Notes

Reaction equation

HRID 1982411 reaction equation
C[O:2][C:3]([C:5]1[O:16][C:15]2[C:14]3[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=3[N:8]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:7]=2[C:6]=1[O:23][CH3:24])=[O:4].[OH-].[Na+].O>CO>[CH3:24][O:23][C:6]1[C:7]2[N:8]([C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)[C:9]3[CH:10]=[CH:11][CH:12]=[CH:13][C:14]=3[C:15]=2[O:16][C:5]=1[C:3]([OH:4])=[O:2]

Participants

5

Procedure

A suspension of 13.5 g (0.042 mole) of 3-methoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxylic acid methyl ester in 75 ml of methanol was treated with 70.6 ml of 1.0 N aqueous sodium hydroxide. The mixture was stirred at reflux for 17 hours, then added to 1.4 l of water. The insoluble material was filtered, added to 1.0 l of water, and acidified with acetic acid while cooling in an ice bath. The crude acid product was recovered by filtration. The original filtrate from the reaction mixture and 1.4 l of water was also cooled in ice and acidified with acetic acid. The crude product obtained was filtered and combined with the earlier crop. The combined crude products were stirred in 400 ml of water, filtered, and recrystallized from methanol. There was obtained 5.8 g (45% yield) of analytically pure acid, mp 154°-155° C.

Workup

  1. temperatureat reflux for 17 hours
  2. filtrationThe insoluble material was filtered
  3. additionadded to 1.0 l of water
  4. temperaturewhile cooling in an ice bath
  5. filtrationThe crude acid product was recovered by filtration
  6. temperatureThe original filtrate from the reaction mixture and 1.4 l of water was also cooled in ice

Sources & evidence

ORD record
ord-f9bfb7ffd30248faa8fd2ea6e673c4a2
Source dataset
uspto-grants-1986_06
Patent number
US04596814

Reaction notes

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