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Ammonia → 3-(Prop-1-EN-2-YL)octan-2-one

HRID 1494694
ノート
印刷プレビュー

反応式

HRID 1494694 の反応式
N.[Na].[NH2-].[Na+].[CH3:5][C:6]([CH3:11])=[CH:7][C:8](=[O:10])[CH3:9].Br[CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]>CCOCC>[CH2:13]([CH:7]([C:6]([CH3:11])=[CH2:5])[C:8](=[O:10])[CH3:9])[CH2:14][CH2:15][CH2:16][CH3:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 222Ammonia2 回HCID 80571-BromopentaneHCID 8858Mesityl oxideHCID 24533Sodium amideHCID 5360545Sodium2 回

生成物 1

HCID 132086193-(Prop-1-EN-2-YL)octan-2-one収率 897.6%

試薬・触媒・溶媒 1

HCID 3283
Diethyl Ether
溶媒
2 回

実験手順

100 ml of liquid ammonia was condensed into a 2-neck flask fitted with a dropping funnel, inlet tube, and dry-ice condenser. A few crystals of ferric chloride were added, followed by the addition of 2.3 g (0.1 mole) of sodium. When the sodium was converted to sodium amide, the deep blue color changed to gray. A solution of 10 g (0.1 mole) of 4-methyl-3-pentene-2-one in 10 ml of ether was added dropwise, resulting in a green-blue solution. After 15 minutes a solution of 1.5 g (1 equivalent) of bromopentane in 5 ml of ether was added, changing the color to light brown. After 1 hour of stirring, the ammonia was allowed to evaporate and ether and water were added. The organic layer was separated, washed with water, washed with two 10 ml portions of 5% HCl, and dried over MgSO4. Evaporation of the ether yielded 15 g (88% yield) of 3-pentyl-4-methyl-4-pentene-2-one: ##STR15##

後処理

  1. customcondensed into a 2-neck flask
  2. customfitted with a dropping funnel, inlet tube, and dry-ice condenser
  3. customresulting in a green-blue solution
  4. customto evaporate
  5. additionether and water were added
  6. customThe organic layer was separated
  7. washwashed with water
  8. washwashed with two 10 ml portions of 5% HCl
  9. dry with materialdried over MgSO4
  10. customEvaporation of the ether

出典と根拠

ORDレコード
ord-2ae6bdf946c947fdad300fa0ebac5d85
出典データセット
uspto-grants-1991_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05026918

反応ノート

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