関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | O-Cresol | HCID 335 | — |
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | 2,6-Dimethylphenol | HCID 11335 | — |
| 反応物 | 2,6-Di-sec-butyl-alpha-methoxy-p-cresol | HCID 20069433 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-[[4-Hydroxy-3,5-bis(1-methylpropyl)phenyl]methyl]-2,6-dimethylphenol | HCID 20237394 | 90% |
反応手順
The procedure of Example 2 was followed using 50.45 grams (0.202 mol) of 2,6-di-sec-butyl-α-methoxy-p-cresol in 30 mL methylene chloride and 39.0 grams (0.320 mol) 2,6-dimethylphenol with 42 grams 78% sulfuric acid. The reaction was carried out at about 8° C. with mechanical stirring. The 2,6-di-sec-butylephenol used to prepare the cresol according to the procedure of Example 3 was of only 85.7 percent purity. Accordingly, the yield of the cresol was only 67% (86.9 area % by gas chromatography). The product of the invention: [4-[[4-hydroxy-3,5-bis(1-methylpropyl)phenyl]methyl]-2,6-dimethylphenol, was obtained as a viscous oil (liquid) at room temperature in 90 percent yield (61.77 grams) (84.4 area percent by gas chromatography). The compound has a pour point of 22° C. (as measured by ASTM test D-97).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04609767 |
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| 出典データセット | uspto-grants-1986_09 |
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| ORD ID | ord-0a22cdc07d984b8a98d59cebc4a9f378 |
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| 出典メモ | uspto-grants-1986_09 |
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