Diethyl Ether → alpha-Allyl-alpha,3,3-trimethyl-2-norbornane-methanol

HRID 1112626

反応式

HRID 1112626 の反応式
[Mg].[CH2:2](Cl)[CH:3]=C.[C:6]([CH:9]1[C:14]([CH3:16])([CH3:15])[CH:13]2[CH2:17][CH:10]1[CH2:11][CH2:12]2)(=[O:8])[CH3:7].[NH4+].[Cl-].[CH3:20]COCC>>[CH2:7]([C:6]([CH3:20])([CH:9]1[C:14]([CH3:16])([CH3:15])[CH:13]2[CH2:17][CH:10]1[CH2:11][CH2:12]2)[OH:8])[CH:2]=[CH2:3]

参加物

6

実験手順

The magnesium turnings are placed into a 1 liter, 3 neck reaction flask, followed by 200 cc of anhydrous ether. Approximately 6 cc of allyl chloride is added to initiate formation of the Grignard reagent. When the reaction is initiated, the remaining allyl chloride is added dropwise over a 2 hour period, with moderate reflux. After the addition, reflux is continued for 1 hour; at which time 28.5 g 2-acetyl-3,3-dimethylnorbornane is introduced over a 20 minute period. The reaction is very exothermic during this addition. At the end of the addition, refluxing is continued for 1 hour. The work is carried out by hydrolyzing with NH4Cl solution, filtering and separating the layers. The organic layer is washed with two 200 cc portions of water, dried over MgSO4, filtered and concentrated to give 34 grams of oil which is distilled to give 26 g of product, b.p. 90°-105° C. at 1-2 mm Hg.

後処理

  1. additionAfter the addition
  2. temperaturereflux
  3. additionThe reaction is very exothermic during this addition
  4. additionAt the end of the addition
  5. temperaturerefluxing
  6. waitis continued for 1 hour
  7. filtrationfiltering
  8. customseparating the layers
  9. washThe organic layer is washed with two 200 cc portions of water
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated

出典と根拠

ORDレコード
ord-d575ff2cfa534746bf67057f5c4b784f
出典データセット
uspto-grants-1978_10
特許番号
US04123393

関連ノート

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