Ethyl 1-propenyl ether → 2-(2-Formylpropyl)-3-isopropenyl-1-methyl-cyclopent-1-ene

HRID 437488

反応式

HRID 437488 の反応式
[C:1]([CH:4]1[CH2:8][CH2:7][C:6]([CH3:10])(O)[C:5]1=[CH2:11])([CH3:3])=[CH2:2].[CH:12]([O:15]CC)=[CH:13][CH3:14]>P(=O)(O)(O)O>[CH:12]([CH:13]([CH3:14])[CH2:11][C:5]1[CH:4]([C:1]([CH3:3])=[CH2:2])[CH2:8][CH2:7][C:6]=1[CH3:10])=[O:15]

参加物

4

実験手順

15 drops of 85% phosphoric acid were added to a mixture, cooled to -30° C in a laboratory autoclave, of 76 g of 3-isopropenyl-1-methyl-2-methylene-cyclopentan-1-ol and 130 g of ethyl 1-propenyl ether. After gassing with nitrogen, the autoclave was brought, in an oil bath of 180° C, to an internal temperature of 150° C (this took about 15 minutes) and held at this temperature until a distinct drop in pressure occurred (about 75 minutes). The reaction mixture was then quenched, taken up in ether, washed with aqueous bicarbonate solution and water, the solution dried over anhydrous magnesium sulphate and concentrated under reduced pressure. The crude product (135 g), obtained as a yellow oil, was fractionated and yielded 64 g (67%) of pure 2-(2-formylpropyl)-3-isopropenyl-1-methyl-cyclopent-1-ene having woody, earthy, musty fragrance; boiling point 0.005 = 51° C; nD20 = 1.4825; IRfilm : νmax = 3090, 2730, 1735, 1645, 1460, 1380 and 898 cm-1.

後処理

  1. customthe autoclave was brought, in an oil bath of 180° C, to an internal temperature of 150° C
  2. customthis took about 15 minutes
  3. custom(about 75 minutes)
  4. customThe reaction mixture was then quenched
  5. washwashed with aqueous bicarbonate solution and water
  6. dry with materialthe solution dried over anhydrous magnesium sulphate
  7. concentrationconcentrated under reduced pressure
  8. customThe crude product (135 g), obtained as a yellow oil

出典と根拠

ORDレコード
ord-2ff6b67204be465e9b852afb903a1b4b
出典データセット
uspto-grants-1977_06
特許番号
US04031132

関連ノート

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