Propargyl alcohol → 2,4-Heptadiyn-1-ol, 6,6-dimethyl-

HRID 580007ノート

反応式

HRID 580007 の反応式
[CH2:1]([OH:4])[C:2]#[CH:3].Br[C:6]#[C:7][C:8]([CH3:11])([CH3:10])[CH3:9].[C-]#N.[K+]>O>[CH3:9][C:8]([CH3:11])([CH3:10])[C:7]#[C:6][C:3]#[C:2][CH2:1][OH:4]

参加物

5

実験手順

Nitrogen was bubbled through a mixture of cupric chloride (154 mg), NH2OH.HCl (0.45 g), and 70% aqueous diethylamine (9 ml) in 11 ml of water and 23 ml of methanol, for a few minutes. Propargyl alcohol (3.8 g, 0.068 mol) was added with stirring under nitrogen whereupon a yellow precipitate formed immediately. The mixture was warmed to 35°-40° C. for 15 minutes and 1-bromo-2-t-butyl-acetylene (8.57 g, 0.053 mmol) was added over 15 minutes. The mixture was stirred at 35°-40° C. for 45 minutes, then at room temperature for 1 hour. Aqueous potassium cyanide (0.45 g in 45 ml of water) was added and the mixture was stirred for one minute. The mixture was poured into 50 ml of water and extracted 5 times with ether. The combined organic phase was washed with water and dried over magnesium sulfate. The solvents were removed and the residue was distilled under reduced pressure through a column packed with glass helices. 6,6-Dimethyl-2,4-heptadiyne-1-ol (3.63 grams) was collected at 85° C. and 0.5 mm of mercury.

後処理

  1. customNitrogen was bubbled through a mixture of cupric chloride (154 mg), NH2OH.HCl (0.45 g), and 70% aqueous diethylamine (9 ml) in 11 ml of water and 23 ml of methanol, for a few minutes
  2. customformed immediately
  3. temperatureThe mixture was warmed to 35°-40° C. for 15 minutes
  4. stirringThe mixture was stirred at 35°-40° C. for 45 minutes
  5. stirringthe mixture was stirred for one minute
  6. extractionextracted 5 times with ether
  7. washThe combined organic phase was washed with water
  8. dry with materialdried over magnesium sulfate
  9. customThe solvents were removed
  10. distillationthe residue was distilled under reduced pressure through a column
  11. custom6,6-Dimethyl-2,4-heptadiyne-1-ol (3.63 grams) was collected at 85° C.

出典と根拠

ORDレコード
ord-8aebcc3e6eff4e9db12589a2692ffb01
出典データセット
uspto-grants-1988_06
特許番号
US04751245

反応ノート

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