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Ethyl Acetate → HCID 86758842、化合物

HRID 1059281
ノート
印刷プレビュー

反応式

HRID 1059281 の反応式
[H-].[Na+].[CH3:3][N:4]1[CH2:10][CH:9]2[C:11](=O)[CH:6]([C@H:7]([CH3:14])[C@H:8]2[CH3:13])[CH2:5]1.[C:15]([O:18][CH2:19][CH3:20])(=[O:17])[CH3:16]>O1CCCC1>[CH3:3][N:4]1[CH2:10][CH:9]2[C:11](=[CH:16][C:15]([O:18][CH2:19][CH3:20])=[O:17])[CH:6]([C@H:7]([CH3:14])[C@H:8]2[CH3:13])[CH2:5]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

5

反応物 3

HCID 8857Ethyl AcetateHCID 24758Sodium hydrideHCID 69884103HCID 69884103、化合物

生成物 1

HCID 86758842HCID 86758842、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

To a solution of 4.35 g of triethyl phosphonoacetate in tetrahydrofuran (50 ml) was added 0.85 g of sodium hydride (oily: 60-72%) under ice-cooling and the resulting mixture was stirred at 0° C. for 10 minutes. Then a solution of 2.7 g of the crude (6R*,7R*)-3,6,7-trimethyl-3-azabicyclo[3.2.1]octan-8-one in tetrahydrofuran (20 ml) was added thereto and the reaction mixture was heated under reflux for 1 hour. After adding ethyl acetate, the reaction mixture was washed with a saturated aqueous solution of sodium chloride and the organic layer was dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate) to thereby give 1.6 g of the title compound as a pale yellow oily substance.

後処理

  1. temperaturecooling
  2. temperaturethe reaction mixture was heated
  3. temperatureunder reflux for 1 hour
  4. washthe reaction mixture was washed with a saturated aqueous solution of sodium chloride
  5. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  6. distillationAfter distilling off the solvent under reduced pressure
  7. customthe residue was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-762f92867a8c4f01a81022eab6ecd2ce
出典データセット
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06518423B1

反応ノート

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