Tetrahydrofuran → HCID 18348647, compound

HRID 2268547Notes

Reaction equation

HRID 2268547 reaction equation
[C:1]1([C:7]2[CH:34]=[CH:33][C:10]([O:11][CH2:12][CH2:13][CH:14]3[CH2:20][CH2:19][C:18]4[C:21]([O:31]C)=[C:22]([O:29][CH3:30])[C:23]([O:27][CH3:28])=[C:24]([O:25]C)[C:17]=4[CH2:16][CH2:15]3)=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.N1C(C(O)=O)=CC=CC=1C(O)=O.C1COCC1.O=[N+]([O-])[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[Ce+4].[NH4+].[NH4+]>O>[CH3:28][O:27][C:23]1[C:24](=[O:25])[C:17]2[CH2:16][CH2:15][CH:14]([CH2:13][CH2:12][O:11][C:10]3[CH:9]=[CH:8][C:7]([C:1]4[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=4)=[CH:34][CH:33]=3)[CH2:20][CH2:19][C:18]=2[C:21](=[O:31])[C:22]=1[O:29][CH3:30]

Participants

6

Procedure

To a mixture of 7-[2-(4-phenylphenoxy)ethyl]-1,2,3,4-tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cycloheptene (1.53 g), 2,6-pyridinedicarboxylic acid (1.66 g), THF (60 ml), and water (15 ml) was dropwise added a solution of CAN (7.24 g) in water (15 ml) with cooling with ice. After the reaction mixture was stirred for 15 min, water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, and dried. The solvent was removed in vacuo. The residue was purified by alumina column chromatography (ethyl acetate) and then with recrystallization from hexane-ethyl acetate to yield the entitled compound (550 mg) as crystals.

Workup

  1. temperaturewith cooling with ice
  2. extractionwas extracted with ethyl acetate
  3. washThe organic layer was washed with water and saturated aqueous sodium chloride
  4. customdried
  5. customThe solvent was removed in vacuo
  6. customThe residue was purified by alumina column chromatography (ethyl acetate)
  7. customwith recrystallization from hexane-ethyl acetate

Sources & evidence

ORD record
ord-c68f96e1fd0f4f679ab0acdebb266eb5
Source dataset
uspto-grants-2001_12
Patent number
US06326369B1

Reaction notes

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