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HRID 1779527作成日:2026年10月26日
Sulfuric Acid → allyl 3-(5-chloro-2H-benzotriazole-2-yl)-5-(1,1-dimethylethyl)-4-hydroxy-benzene propanate
https://huagongshe.com/reaction/1779527
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Octyl 5-tert-butyl-3-(5-chloro-2H-benzotriazole-2-yl)-4-hydroxybenzenepropionate | HCID 174297 | — |
| 溶媒 | Allyl Alcohol | HCID 7858 | — |
| 生成物 | allyl 3-(5-chloro-2H-benzotriazole-2-yl)-5-(1,1-dimethylethyl)-4-hydroxy-benzene propanate | HCID 20764418 | 90% |
反応手順
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%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05627227 |
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| 出典データセット | uspto-grants-1997_05 |
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| ORD ID | ord-bbfc0c79f8424822a073d8cf55863fcf |
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| 出典メモ | uspto-grants-1997_05 |
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