Toluene → HCID 68114824、化合物

HRID 1731464

反応式

HRID 1731464 の反応式
[CH2:1]([CH:6]([CH2:9][OH:10])[CH2:7][OH:8])[CH2:2][CH2:3][CH:4]=[CH2:5].[CH2:11]([O:15][C:16]1[CH:23]=[CH:22][C:19](C=O)=[CH:18][CH:17]=1)[CH2:12][CH2:13][CH3:14].[C:24]1(C)C=CC=CC=1>S(=O)(=O)(O)O>[CH2:11]([O:15][C:16]1[CH:23]=[CH:22][C:19]([C@H:7]2[C@H:6]([CH2:1][CH2:2][CH2:3][CH:4]=[CH2:5])[CH2:9][O:10][CH2:24][O:8]2)=[CH:18][CH:17]=1)[CH2:12][CH2:13][CH3:14]

参加物

5

実験手順

A mixture of 3.6 g of 2-(4-pentenyl)-1,3-propanediol, 4.4 g of p-butoxybenzaldehyde, 75 ml of toluene and 3 drops of 10% sulphuric acid was heated to boiling for 2.5 hours, whereby about 50 ml of wet solvent were distilled off and were replaced by the dropwise addition of 50 ml of fresh toluene. Thereafter, the mixture was neutralized with 4 drops of triethylamine and, after cooling, was extracted twice with 50 ml of 5% sodium hydrogen carbonate solution each time and twice with 50 ml of water each time. The organic phase was dried over sodium sulphate and concentrated. The residue (7.5 g) was chromatographed on silica gel with hexane/ethyl acetate (vol. 92:8), whereby 4.2 g of trans-4-(p-butoxyphenyl)-5-(4-pentenyl)-m-dioxane were obtained. Two-fold recrystallization from hexane gave 2.2 g of pure product with m.p. (C--N) 29.5° C. and cl.p. (N--I) 30.7° C.

後処理

  1. temperaturewas heated
  2. distillationwhereby about 50 ml of wet solvent were distilled off
  3. additionwere replaced by the dropwise addition of 50 ml of fresh toluene
  4. temperatureafter cooling
  5. extractionwas extracted twice with 50 ml of 5% sodium hydrogen carbonate solution each time
  6. dry with materialThe organic phase was dried over sodium sulphate
  7. concentrationconcentrated
  8. customThe residue (7.5 g) was chromatographed on silica gel with hexane/ethyl acetate (vol. 92:8)

出典と根拠

ORDレコード
ord-e9f5eada490d470187f7cf0ced484d5d
出典データセット
uspto-grants-1986_11
特許番号
US04621901

関連ノート

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