Sulfuric Acid → HCID 22729011、化合物

HRID 2085172ノート

反応式

HRID 2085172 の反応式
[CH3:1][C:2](=[N:4][OH:5])[CH3:3].C([Li])CCC.[CH3:11][O:12][C:13]1[C:21]2[CH:20]=[C:19]([C:22](OC)=O)[O:18][C:17]=2[CH:16]=[CH:15][CH:14]=1.S(=O)(=O)(O)O.C(=O)([O-])O.[Na+]>C1COCC1>[CH3:11][O:12][C:13]1[C:21]2[CH:20]=[C:19]([C:22]3[O:5][N:4]=[C:2]([CH3:3])[CH:1]=3)[O:18][C:17]=2[CH:16]=[CH:15][CH:14]=1

参加物

7

反応物 5

HCID 1118Sulfuric AcidHCID 67180Acetone, oximeHCID 516892Sodium BicarbonateHCID 22729192Methyl 4-methoxybenzofuran-2-carboxylateHCID 178418339Butyllithium

生成物 1

HCID 22729011HCID 22729011、化合物収率 40.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution (160 ml) of acetone oxime (5.0 g) in THF was added dropwise n-butyllithium (1.6 M hexane solution) over 15 min under ice-cooling and the mixture was stirred for 1 hr. Thereto was added dropwise a solution (60 ml) of methyl 4-methoxybenzo(b)furan-2-carboxylate (6.7 g) in THF and the mixture was stirred at room temperature for 2 hr. The reaction mixture was poured into ice water, and conc. sulfuric acid (4 ml) was added carefully. The mixture was stirred for 20 min more. The aqueous layer was neutralized with sodium hydrogencarbonate and extracted with ethyl acetate. After washing with water, the organic layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure to give the title compound (3.0 g) as yellow crystals.

後処理

  1. temperaturecooling
  2. stirringthe mixture was stirred at room temperature for 2 hr
  3. additionwas added carefully
  4. stirringThe mixture was stirred for 20 min more
  5. extractionextracted with ethyl acetate
  6. washAfter washing with water
  7. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  8. customthe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-89fbf8ae90f54bac8472ead640f59394
出典データセット
uspto-grants-2004_04
特許番号
US06720320B2

反応ノート

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