Water → 5-Benzoyl-furan-2-carboxylic acid methyl ester

HRID 1935610Notes

Reaction equation

HRID 1935610 reaction equation
[C:1](Cl)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:10][O:11][C:12]([C:14]1[O:15][CH:16]=[CH:17][CH:18]=1)=[O:13].O>C(Cl)(Cl)(Cl)Cl>[C:2]1([C:1]([C:16]2[O:15][C:14]([C:12]([O:11][CH3:10])=[O:13])=[CH:18][CH:17]=2)=[O:8])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

5

Procedure

Anhydrous ferric chloride (0.42 g, 2.6 mmole) and benzoyl chloride (29.6 g, 0.21 mole), were dissolved in CCl4 (40 mL) and added dropwise over 10 min with methyl-2-furoate (25.2 g, 0.20 mmole). The reaction mixture was then heated under reflux for 36 hours, and after cooling was added with water (120 mL). The mixture was stirred for 1 hour and then allowed to sit until it separated into two layers. The water layer and precipitate were extracted with chloroform. The chloroform extract was dried over anhydrous magnesium sulfate and then filtered. The solvent of the filtrate was removed under a reduced pressure; the residue was recrystallized from isopropanol to afford 28.4 g 5-methoxycarbonyl-2-furyl phenyl ketone in a yield of 65.0%.

Workup

  1. temperatureThe reaction mixture was then heated
  2. temperatureunder reflux for 36 hours
  3. temperatureafter cooling
  4. customseparated into two layers
  5. extractionThe water layer and precipitate were extracted with chloroform
  6. extractionThe chloroform extract
  7. dry with materialwas dried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. customThe solvent of the filtrate was removed under a reduced pressure
  10. customthe residue was recrystallized from isopropanol

Sources & evidence

ORD record
ord-5983529184434aacae6eaebd32225eba
Source dataset
uspto-grants-2002_05
Patent number
US06387942B2

Reaction notes

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