Dimethylformamide → HCID 69128292, compound

HRID 1960204Notes

Reaction equation

HRID 1960204 reaction equation
[CH2:1]([SH:3])[CH3:2].CN(C=O)C.[H-].[Na+].O([CH:18]=[CH:19][C:20](=[N:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[O:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)C1C=CC=CC=1>C(OCC)(=O)C>[CH2:1]([S:3][CH:18]=[CH:19][C:20](=[N:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[O:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[CH3:2]

Participants

6

Reactant 4

HCID 6228Dimethylformamide2×HCID 6343EthanethiolHCID 24758Sodium hydrideHCID 69127142Phenyl 3-phenoxy-N-phenylacrylimidate

Product 1

HCID 69128292HCID 69128292, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

Ethanethiol (0.11 ml) was dissolved to DMF (3 ml), and sodium hydride (60% in oil: 60 mg) was added under ice-cooling, and stirred for 30 minutes at the same temperature. Phenyl 3-phenoxy-N-phenylacrylimidate (0.30 g) was dissolved to DMF (2 ml), and the obtained solution was added to the above mentioned thiolate solution under ice-cooling, and stirred for two hours at the same temperature and for two hours at room temperature. Ethyl acetate (100 ml) was added to the reaction solution, and it was successively washed with 1N aqueous sodium hydroxide solution, water and aqueous saturated sodium chloride solution, dried over magnesium sulfate (anhydrous), concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain phenyl 3-ethylthio-N-phenylacrylimidate (0.14 g) as yellow oil.

Workup

  1. additionwas added under ice-
  2. temperaturecooling
  3. additionthe obtained solution was added to the
  4. temperaturecooling
  5. stirringstirred for two hours at the same temperature and for two hours at room temperature
  6. washwas successively washed with 1N aqueous sodium hydroxide solution, water and aqueous saturated sodium chloride solution
  7. dry with materialdried over magnesium sulfate (anhydrous)
  8. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-c30ffe4c27c44a9a84e52b11fc02fb3c
Source dataset
uspto-grants-2013_04
Patent number
US08410316B2

Reaction notes

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