Dimethylformamide → HCID 86617329, compound

HRID 661744Notes

Reaction equation

HRID 661744 reaction equation
C(=O)([O-])[O-].[K+].[K+].[C:7](Cl)(=[O:9])[CH3:8].CN(C=O)C.[OH:16][C:17]1[CH:22]=[CH:21][C:20]([N:23]=[C:24]([O:34][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)[CH:25]=[CH:26][O:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[CH:19][CH:18]=1>COC(C)(C)C>[C:7]([O:16][C:17]1[CH:22]=[CH:21][C:20]([N:23]=[C:24]([O:34][C:35]2[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=2)[CH:25]=[CH:26][O:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[CH:19][CH:18]=1)(=[O:9])[CH3:8]

Participants

6

Procedure

Potassium carbonate (0.075 g) and acetyl chloride (0.035 ml) were added to DMF (3 ml) solution of phenyl N-(4-hydroxyphenyl)-3-(phenoxy)acrylimidate (0.15 g) at room temperature and stirred for two hours at the same temperature and for three hours at 50° C. t-Butyl methyl ether (80 ml) was added to the reaction solution, and it was successively washed with water and aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, concentrated under reduced pressure. The residue was separated and purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to obtain phenyl N-(4-acetoxyphenyl)-3-(phenoxy)acrylimidate (0.11 g) as colorless oil.

Workup

  1. additionwas added to the reaction solution, and it
  2. washwas successively washed with water and aqueous saturated sodium chloride solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was separated
  6. custompurified by silica gel column chromatography (hexane:ethyl acetate=4:1)

Sources & evidence

ORD record
ord-1297e18f11754ab6bbb53632cbbc2cce
Source dataset
uspto-grants-2011_12
Patent number
US08084644B2

Reaction notes

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