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

HRID 2355142Notes

Reaction equation

HRID 2355142 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 of 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-fdbe338bc04845e097d2caf43cc0d61f
Source dataset
uspto-grants-2010_07
Patent number
US07754751B2

Reaction notes

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