反応式
[Cl:1][C:2]1[CH:34]=[CH:33][C:5]2=[N:6][N:7]([C:9]3[CH:10]=[C:11]([CH2:20][CH2:21][C:22]([O:24][CH2:25][CH2:26][CH2:27]CCCCC)=[O:23])[CH:12]=[C:13]([C:16]([CH3:19])([CH3:18])[CH3:17])[C:14]=3[OH:15])[N:8]=[C:4]2[CH:3]=1.S(=O)(=O)(O)O>C(O)C=C>[Cl:1][C:2]1[CH:34]=[CH:33][C:5]2=[N:6][N:7]([C:9]3[CH:10]=[C:11]([CH2:20][CH2:21][C:22]([O:24][CH2:25][CH:26]=[CH2:27])=[O:23])[CH:12]=[C:13]([C:16]([CH3:17])([CH3:18])[CH3:19])[C:14]=3[OH:15])[N:8]=[C:4]2[CH:3]=1参加物
実験手順
220 g (0.45 mol) of octyl 3-(5-chloro-2H-benzotriazole-2-yl)-5-(1,1-dimethylethyl)-4-hydroxy-benzene propanate manufactured by CIBA GEIGY INC. under the trade name of "TINUVIN 109" were dissolved in 500 ml of allyl alcohol, and was admixed with 5 ml of concentrated sulfuric acid. The resulting solution was refluxed for five hours. After cooling, a precipitated product was filtered off. The resulting solid substance was dissolved in 300 ml of methylene chloride, washed with a saturated aqueous solution of NaHCO3 and dried over magnesium sulfate. After filtration, the solvent was distilled off and the resulting solid substance was recrystallized from hexane to produce allyl 3-(5-chloro-2H-benzotriazole-2-yl)-5-(1,1-dimethylethyl)-4-hydroxy-benzene propanate, referred to hereinafter as a precursor (4) at a yield of 90%.
後処理
- temperatureThe resulting solution was refluxed for five hours
- temperatureAfter cooling
- filtrationa precipitated product was filtered off
- dissolutionThe resulting solid substance was dissolved in 300 ml of methylene chloride
- washwashed with a saturated aqueous solution of NaHCO3
- dry with materialdried over magnesium sulfate
- filtrationAfter filtration
- distillationthe solvent was distilled off
- customthe resulting solid substance was recrystallized from hexane
出典と根拠
- ORDレコード
- ord-bbfc0c79f8424822a073d8cf55863fcf
- 出典データセット
- uspto-grants-1997_05
- 特許番号
- US05627227
関連ノート
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