Water → Methyl 4-cyano-3-methoxybenzoate

HRID 550275ノート

反応式

HRID 550275 の反応式
[CH:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][C:4]=1[O:13][CH3:14])=O.Cl.[NH2:16]O.O.C(=O)([O-])O.[Na+]>C(O)=O>[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][C:4]=1[O:13][CH3:14])#[N:16]

参加物

6

反応物 4

HCID 962WaterHCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 10631650Methyl 4-formyl-3-methoxybenzoate

生成物 1

HCID 22464400Methyl 4-cyano-3-methoxybenzoate収率 91.1%

試薬・触媒・溶媒 1

HCID 284Formic Acid溶媒

実験手順

To a solution (20 ml) of methyl 4-formyl-3-methoxybenzoate (870 mg, 4.48 mmol) in formic acid was added hydroxylamine hydrochloride (405 mg, 5.82 mmol), and the mixture was stirred at room temperature for 1 hr. The temperature was raised to 50° C., and the mixture was further stirred for 24 hrs. Water was added to the reaction mixture, the mixture was neutralized with saturated aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The extract was dried over anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with hexane-ethyl acetate (1:0-7:3, v/v) to give the title compound (780 mg, 91%) as a colorless oil.

後処理

  1. temperatureThe temperature was raised to 50° C.
  2. stirringthe mixture was further stirred for 24 hrs
  3. extractionextracted with ethyl acetate
  4. dry with materialThe extract was dried over anhydrous MgSO4
  5. customthe solvent was evaporated under reduced pressure
  6. washeluted with hexane-ethyl acetate (1:0-7:3

出典と根拠

ORDレコード
ord-a983fe77be69471392b0b10ee231d92f
出典データセット
uspto-grants-2011_05
特許番号
US07943770B2

反応ノート

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