Potassium Carbonate → 3-(4-tert-butylphenyl)-N-(3,4-dimethoxyphenyl)acrylamide

HRID 2105562ノート

反応式

HRID 2105562 の反応式
[C:1]([C:5]1[CH:15]=[CH:14][C:8](/[CH:9]=[CH:10]/[C:11]([OH:13])=O)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].C(Cl)(=O)C(Cl)=O.[CH3:22][O:23][C:24]1[CH:25]=[C:26]([CH:28]=[CH:29][C:30]=1[O:31][CH3:32])[NH2:27].C(=O)([O-])[O-].[K+].[K+]>CCOC(C)=O.CC(C)=O.O.CN(C=O)C.C(Cl)Cl>[CH3:22][O:23][C:24]1[CH:25]=[C:26]([NH:27][C:11](=[O:13])/[CH:10]=[CH:9]/[C:8]2[CH:7]=[CH:6][C:5]([C:1]([CH3:2])([CH3:3])[CH3:4])=[CH:15][CH:14]=2)[CH:28]=[CH:29][C:30]=1[O:31][CH3:32]

参加物

10

反応物 4

HCID 11430Potassium CarbonateHCID 227703,4-DimethoxyanilineHCID 65578Oxalyl chlorideHCID 7248394-(Tert-butyl)cinnamic acid

生成物 1

HCID 101499553-(4-tert-butylphenyl)-N-(3,4-dimethoxyphenyl)acrylamide

試薬・触媒・溶媒 5

HCID 180Acetone溶媒HCID 962Water溶媒HCID 6228Dimethylformamide溶媒HCID 6344Dichloromethane溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a 20 mL round-bottomed flask equipped with reflux condenser and drying tube was added 4-tert-butyl-trans-cinnamic acid (200 mg, 0.98 mmol, EMKA-Chemie) followed by CH2Cl2 (5 mL), oxalyl chloride (90 uL, 130 mg, 1.03 mmol, Aldrich) and DMF (1 uL). The reaction mixture was magnetically stirred and heated at reflux for 30 min. The reaction mixture was concentrated in vacuo and the residue dissolved in acetone (2 mL). The solution was added to a mixture of 3,4-dimethoxyaniline (180 mg, 1.17 mmol, Aldrich), potassium carbonate (200 mg), water (2 mL) and acetone (2 mL), magnetically stirred at 25° C. in a 10 mL glass vial. The reaction mixture was stirred at 25° C. for 16 h then diluted with EtOAc (60 mL) and washed successively with 1 N HCl (20 mL), 1 N NaOH (20 mL), water (20 mL) and satd NaCl (20 mL), dried over MgSO4, filtered and concentrated. Recrystallization from hexane and CH2Cl2 provided the title product as a yellow solid. MP 115-116° C. MS (ESI, pos. ion) m/z: 340 (M+1).

後処理

  1. customTo a 20 mL round-bottomed flask equipped
  2. temperaturewith reflux condenser
  3. customdrying tube
  4. temperatureheated
  5. temperatureat reflux for 30 min
  6. concentrationThe reaction mixture was concentrated in vacuo
  7. dissolutionthe residue dissolved in acetone (2 mL)
  8. stirringThe reaction mixture was stirred at 25° C. for 16 h
  9. washwashed successively with 1 N HCl (20 mL), 1 N NaOH (20 mL), water (20 mL) and satd NaCl (20 mL)
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated
  13. customRecrystallization from hexane and CH2Cl2

出典と根拠

ORDレコード
ord-faf8de176dfd40b2813fe5c59e826d43
出典データセット
uspto-grants-2009_08
特許番号
US07579347B2

反応ノート

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