Sodium amide → 2-(2,3-Dimethoxyphenyl)ethenyl methyl ether

HRID 1006060Notes

Reaction equation

HRID 1006060 reaction equation
[Br-].[CH3:2][O:3][CH2:4][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[NH2-].[Na+].[CH3:26][O:27][C:28]1[C:35]([O:36][CH3:37])=[CH:34][CH:33]=[CH:32][C:29]=1[CH:30]=O>C1COCC1.O>[CH3:2][O:3][CH:4]=[CH:30][C:29]1[CH:32]=[CH:33][CH:34]=[C:35]([O:36][CH3:37])[C:28]=1[O:27][CH3:26]

Participants

6

Procedure

THF (15 mL) was added to a mixture of methoxymethyltriphenylphosphonium bromide and sodium amide (mfd. by Aldrich Chemical Co.; 3.0 g, 6.9 mmol) at room temperature and stirred for 15 minutes. To the resulting orange-colored suspension was added a solution of 2,3-dimethoxybenzaldehyde (997 mg, 6.00 mmol) in THF (5 mL), and stirred for 3 hours. The reaction mixture was diluted with water and extracted three times with ethyl acetate. The extract solution was washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified by the use of a silica gel column (silica gel 50 mL; hexane/ethyl acetate=1/0 to 15/1) to obtain 2-(2,3-dimethoxyphenyl)ethenyl methyl ether (808 mg, 83%) as a yellow oil.

Workup

  1. stirringstirred for 3 hours
  2. extractionextracted three times with ethyl acetate
  3. washThe extract solution was washed with a saturated aqueous sodium chloride solution
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by the use of a silica gel column (silica gel 50 mL; hexane/ethyl acetate=1/0 to 15/1)

Sources & evidence

ORD record
ord-0ccb62134a8d47a4a4bcdd42fca2a7de
Source dataset
uspto-grants-2004_09
Patent number
US06787560B2

Reaction notes

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