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1,1-Dimethoxyethyl(dimethyl)amine → 3-(3-Methyl-1,2,4-oxadiazol-5-yl)benzaldehyde

HRID 1267121
ノート
印刷プレビュー

反応式

HRID 1267121 の反応式
O1CC[O:3][CH:2]1[C:6]1[CH:7]=[C:8]([CH:12]=[CH:13][CH:14]=1)[C:9]([NH2:11])=[O:10].CO[C:17](OC)([N:19](C)C)[CH3:18]>>[CH3:18][C:17]1[N:11]=[C:9]([C:8]2[CH:7]=[C:6]([CH:14]=[CH:13][CH:12]=2)[CH:2]=[O:3])[O:10][N:19]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 878351,1-Dimethoxyethyl(dimethyl)amineHCID 18545471HCID 18545471、化合物

生成物 1

HCID 185455103-(3-Methyl-1,2,4-oxadiazol-5-yl)benzaldehyde収率 102.7%

反応条件

温度
90 °C

実験手順

A mixture of 3-[1,3]dioxolan-2-yl-benzamide (2.3 g) and dimethylacetamide dimethylacetal (4 g) was heated under reflux for 1 hour and then evaporated to dryness. The oily residue was dissolved in dioxane (20 mL) and hydroxylamine hydrochloride (1.18 g), acetic acid (20 mL) and a 2N aqueous sodium hydroxide solution (9 mL) were added and the mixture was heated at 90° C. for 2 hours. After evaporation, the residue was dissolved in toluene (100 mL) and a 1N hydrochloric acid solution (50 mL) was added and the mixture was stirred at reflux for 2 hours. After cooling at room temperature the organic phase was decanted, washed with water, dried over Na2SO4, filtered and evaporated to give the title compound (2.3 g) as a white solid.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 1 hour
  3. customevaporated to dryness
  4. dissolutionThe oily residue was dissolved in dioxane (20 mL)
  5. additionhydroxylamine hydrochloride (1.18 g), acetic acid (20 mL) and a 2N aqueous sodium hydroxide solution (9 mL) were added
  6. customAfter evaporation
  7. dissolutionthe residue was dissolved in toluene (100 mL)
  8. additiona 1N hydrochloric acid solution (50 mL) was added
  9. temperatureat reflux for 2 hours
  10. temperatureAfter cooling at room temperature the organic phase
  11. customwas decanted
  12. washwashed with water
  13. dry with materialdried over Na2SO4
  14. filtrationfiltered
  15. customevaporated

出典と根拠

ORDレコード
ord-627812b91be54b5c8e9f2a7ad0539939
出典データセット
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06552022B1

反応ノート

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