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Sodium ethoxide → HCID 68515561、化合物

HRID 1717289
ノート
印刷プレビュー

反応式

HRID 1717289 の反応式
[CH3:1][C:2]([CH3:12])=[CH:3][C:4](=O)[CH2:5][C:6]([O:8]CC)=[O:7].[N:13]([C:16]1[CH:26]=[CH:25][C:19]([C:20]([NH:22][CH2:23][CH3:24])=[O:21])=[CH:18][CH:17]=1)=[N+:14]=[N-:15].[O-]CC.[Na+]>C(O)C>[CH2:23]([NH:22][C:20]([C:19]1[CH:25]=[CH:26][C:16]([N:13]2[C:4]([CH:3]=[C:2]([CH3:1])[CH3:12])=[C:5]([C:6]([OH:8])=[O:7])[N:15]=[N:14]2)=[CH:17][CH:18]=1)=[O:21])[CH3:24]
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

5

反応物 3

HCID 2723922Sodium ethoxideHCID 15564232Ethyl 5-methyl-3-oxohex-4-enoateHCID 594322264-azido-N-ethylbenzamide

生成物 1

HCID 68515561HCID 68515561、化合物収率 78.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
50 °C

実験手順

Ethyl 5-methyl-3-oxo-4-hexenoate (1.10 g, 6.56 mmol, 1.1 eq.) obtained in Example 95a) and 4-azido-N-ethylbenzamide (purity 90%, 1.23 g, 5.82 mmol) were dissolved in ethanol (25 ml), sodium ethoxide (550 mg, 7.82 mmol, 1.25 eq.) was added, and the mixture was stirred at room temperature for 30 min and at 50° C. for 10.5 hr. Ethanol was evaporated from the reaction mixture, and the residue was diluted with 2% aqueous sodium carbonate solution (40 ml) and washed with ethyl acetate (40 ml). The organic layer was extracted with 2% aqueous sodium carbonate solution (15 ml). The aqueous layers were combined, washed with ethyl acetate-hexane (2:1, 50 ml), acidified (pH<3) with 6N hydrochloric acid and extracted three times with ethyl acetate (50 ml) and ethyl acetate-THF (3:1, 40 ml). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated, and ethyl acetate was added. The precipitate was collected by filtration, washed with ethyl acetate and diethyl ether and dried to give the title compound as a grayish white powder (1.43 g, 4.55 mmol, 78.2%).

後処理

  1. customEthanol was evaporated from the reaction mixture
  2. additionthe residue was diluted with 2% aqueous sodium carbonate solution (40 ml)
  3. washwashed with ethyl acetate (40 ml)
  4. extractionThe organic layer was extracted with 2% aqueous sodium carbonate solution (15 ml)
  5. washwashed with ethyl acetate-hexane (2:1, 50 ml)
  6. extractionextracted three times with ethyl acetate (50 ml) and ethyl acetate-THF (3:1, 40 ml)
  7. washwashed with saturated brine
  8. dry with materialdried over anhydrous sodium sulfate
  9. concentrationconcentrated
  10. additionethyl acetate was added
  11. filtrationThe precipitate was collected by filtration
  12. washwashed with ethyl acetate and diethyl ether
  13. customdried

出典と根拠

ORDレコード
ord-b87e60d71d604214bc6a8beced7c9519
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07803822B2

反応ノート

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