Ethyl Acetate → HCID 23353164、化合物

HRID 234899

反応式

HRID 234899 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([O:10][CH3:11])=[O:9])=[CH:4][C:3]=1[OH:12].C(OCC)(=O)C.C(=O)([O-])O.[Na+].Br[CH:25]([CH2:29][CH3:30])[C:26](Br)=[O:27]>O>[CH2:29]([CH:25]1[C:26](=[O:27])[NH:1][C:2]2[CH:7]=[CH:6][C:5]([C:8]([O:10][CH3:11])=[O:9])=[CH:4][C:3]=2[O:12]1)[CH3:30]

参加物

6

反応物 4

HCID 8857Ethyl AcetateHCID 1172932-Bromobutanoyl bromideHCID 516892Sodium BicarbonateHCID 7020619Benzoic acid, 4-amino-3-hydroxy-, methyl ester

生成物 1

HCID 23353164HCID 23353164、化合物収率 87%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a solution of 2-amino-5-methoxycarbonylphenol [Tetrahedron, 46(15), 5177-5186 (1990)] (9.80 g) in a mixed solvent of ethyl acetate (200 ml) and water (200 ml) were added sodium hydrogen carbonate (7.30 g) and 2-bromobutyryl bromide (13.70 g) and the mixture was stirred at room temperature for 10 minutes. The organic layer was separated and the solvent was distilled off under reduced pressure. The resulting residue was dissolved in dimethylformamide (500 ml), to the solution was added potassium carbonate (8.90 g) and the mixture was stirred at room temperature for a day. The reaction solution was poured into water to give precipitates, which were taken by filtration and dried to give 2-ethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (12.0 g).

後処理

  1. customThe organic layer was separated
  2. distillationthe solvent was distilled off under reduced pressure
  3. dissolutionThe resulting residue was dissolved in dimethylformamide (500 ml), to the solution
  4. additionwas added potassium carbonate (8.90 g)
  5. stirringthe mixture was stirred at room temperature for a day
  6. additionThe reaction solution was poured into water
  7. customto give
  8. customprecipitates
  9. filtrationwhich were taken by filtration
  10. customdried

出典と根拠

ORDレコード
ord-3f799eee7bde4f37b8c1e0686a48f40d
出典データセット
uspto-grants-1997_01
特許番号
US05597820

関連ノート

読み込み中…