Triphenylsilanol → (2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehyde

HRID 2051056

反応式

HRID 2051056 の反応式
C1([Si](C2C=CC=CC=2)(C2C=CC=CC=2)[OH:8])C=CC=CC=1.[CH3:21][C:22]1[C:27](O)([C:28]#[CH:29])[C:26]([CH3:32])([CH3:31])[CH2:25][C:24](=[O:33])[CH:23]=1>C1(C)C(C)=CC=CC=1.[V].C(O)(=O)CCCCCCCCCCCCCCCCC>[CH3:21][C:22]1[C:27](=[CH:28][CH:29]=[O:8])[C:26]([CH3:32])([CH3:31])[CH2:25][C:24](=[O:33])[CH:23]=1

参加物

6

実験手順

Triphenylsilanol (22 g) and 80 g (0.45 mol) of 3,5,5-trimethyl-4-hydroxy-4-ethynylcyclohex-2-en-1-one and 1.6 g of stearic acid are dissolved in 800 ml of xylene, treated with 1.92 ml of vanadium isopropylate and heated to reflux temperature while stirring. After 31/2 hours the reaction mixture is cooled and washed with 5% sodium bicarbonate, whereby an emulsion results. The organic phase is then separated, the emulsion is also separated and extracted with ether. The organic phases are dried over magnesium sulphate and concentrated. The residue (117.9 g) is distilled (oil bath 130°-170°; 0.001 mm Hg). In this manner there are obtained 51.8 g (64.8%) of (2,6,6-trimethyl-4-oxo-2-cyclohexen-1-ylidene)acetaldehyde (Z:E=about 3:1).

後処理

  1. temperatureheated
  2. temperatureto reflux temperature
  3. temperatureAfter 31/2 hours the reaction mixture is cooled
  4. washwashed with 5% sodium bicarbonate, whereby an emulsion
  5. customresults
  6. customThe organic phase is then separated
  7. customthe emulsion is also separated
  8. extractionextracted with ether
  9. dry with materialThe organic phases are dried over magnesium sulphate
  10. concentrationconcentrated
  11. distillationThe residue (117.9 g) is distilled (oil bath 130°-170°; 0.001 mm Hg)

出典と根拠

ORDレコード
ord-0359fddf0abb462580cf59fabb0bbe63
出典データセット
uspto-grants-1991_05
特許番号
US05015779

関連ノート

読み込み中…