Dihydrobenzofuran → 4-(2,3-Dihydro-5-benzofuranyl)-4-oxo-2-trifluoroacetamidobutanoic acid

HRID 2352045Notes

Reaction equation

HRID 2352045 reaction equation
[F:1][C:2]([F:14])([F:13])[C:3]([NH:5][C@@H:6]1[C:11](=[O:12])[O:10][C:8](=[O:9])[CH2:7]1)=[O:4].[Cl-].[Al+3].[Cl-].[Cl-].[O:19]1[C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=2[CH2:21][CH2:20]1.[Cl-].[NH4+]>ClC(Cl)C>[O:19]1[C:23]2[CH:24]=[CH:25][C:26]([C:8](=[O:9])[CH2:7][CH:6]([NH:5][C:3](=[O:4])[C:2]([F:1])([F:14])[F:13])[C:11]([OH:12])=[O:10])=[CH:27][C:22]=2[CH2:21][CH2:20]1

Participants

6

Procedure

0.1 mole of the compound obtained in Example 1 and 0.05 mole of aluminum chloride suspended in 100 ml of dichloroethane are added to a solution of 12 ml of dichloroethane containing 0.05 mole of 2,3-dihydrobenzofuran. The mixture is stirred for 36 hours at room temperature and then hydrolyzed with saturated ammonium chloride solution. The mixture is extracted with dichloromethane and the extract washed with water, dried over magnesium sulfate, filtered and concentrated to obtain the expected product.

Workup

  1. extractionThe mixture is extracted with dichloromethane
  2. washthe extract washed with water
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-51a604d4bea14f7d938a088ac7528e4e
Source dataset
uspto-grants-1989_10
Patent number
US04874878

Reaction notes

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