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Hydrogen Peroxide → HCID 59226035、化合物

HRID 2370278
ノート
印刷プレビュー

反応式

HRID 2370278 の反応式
B1C2CCCC1CCC2.[C:10]([O:14][C:15](=[O:34])[NH:16][C:17]1([CH2:31][CH:32]=[CH2:33])[CH2:22][CH2:21][CH:20]([O:23][Si:24]([C:27]([CH3:30])([CH3:29])[CH3:28])([CH3:26])[CH3:25])[CH2:19][CH2:18]1)([CH3:13])([CH3:12])[CH3:11].[OH-:35].[Na+].OO>C1COCC1>[C:10]([O:14][C:15](=[O:34])[NH:16][C:17]1([CH2:31][CH2:32][CH2:33][OH:35])[CH2:22][CH2:21][CH:20]([O:23][Si:24]([C:27]([CH3:30])([CH3:29])[CH3:28])([CH3:25])[CH3:26])[CH2:19][CH2:18]1)([CH3:13])([CH3:12])[CH3:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 789669-Borabicyclo(3.3.1)nonaneHCID 59226056HCID 59226056、化合物

生成物 1

HCID 59226035HCID 59226035、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

16.2 mL (8.12 mmol) of a 0.5M solution of 9-BBN in THF were added to a solution of 1.00 g (2.71 mmol) of [1-allyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclohexyl]-carbamic acid tert-butyl ester (31) in 5 mL THF at 0° C. The reaction mixture was allowed to warm to room temperature over night, before being cooled to 0° C. Then, 20 mL of 3M aqueous sodium hydroxide and 20 mL of 30% aqueous hydrogen peroxide were added slowly, and the mixture was stirred for 12 h. The mixture was extracted twice with ethyl acetate, washed with water and saturated sodium chloride solution, dried over magnesium sulfate and concentrated in vacuo. 0.85 g of the title compound 32 could be isolated as mixture of diastereoisomers in a purity sufficient for further conversion. Rt=2.03 min, 2.10 min (Method C). Detected mass: 388.3 (M+H+).

後処理

  1. temperaturebefore being cooled to 0° C
  2. extractionThe mixture was extracted twice with ethyl acetate
  3. washwashed with water and saturated sodium chloride solution
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-3914bcb7932c4a3d87d35b0a3c7044f5
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08710077B2

反応ノート

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