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

HRID 2164335노트

반응식

HRID 2164335 반응식
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]

참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 13220385HCID 13220385, 화합물

생성물 1

HCID 132203943-Methoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxylic acid수율 45%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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 1.0N 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 are obtained 5.8 g (45% yield) of analytically pure acid, mp 154°-155° C.

후처리

  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

출처 및 근거

ORD 기록
ord-ff75efe93967467383a97ed42f11bd65
출처 데이터셋
uspto-grants-1985_03
특허 번호
US04503236

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