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
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
- temperaturewas heated
- distillationwhereby about 50 ml of wet solvent were distilled off
- additionwere replaced by the dropwise addition of 50 ml of fresh toluene
- temperatureafter cooling
- extractionwas extracted twice with 50 ml of 5% sodium hydrogen carbonate solution each time
- dry with materialThe organic phase was dried over sodium sulphate
- concentrationconcentrated
- 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-548bcd68c9294176a6facae08e2fe17b
- 出典データセット
- uspto-grants-1987_11
- 特許番号
- US04709030
関連ノート
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