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2,6-Di-tert-butylhydroquinone → 2,6-Di(t-butyl)-4-hydroxy-4-(2'-methoxyphenyl)-2,5-cyclohexadienone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,6-Di-tert-butylhydroquinone | HCID 75550 | — |
| 反応物 | p-Bromo methoxybenzene | HCID 13097734 | — |
| 生成物 | 2,6-Di(t-butyl)-4-hydroxy-4-(2'-methoxyphenyl)-2,5-cyclohexadienone | HCID 23333204 | — |
反応手順
Using the method described in Example 1, 2-bromomethoxybenzene is reacted with 2,6-di(t-butyl)hydroquinone to provide 2,6-di(t-butyl)-4-hydroxy-4-(2'-methoxyphenyl)-2,5-cyclohexadienone. This product is dissolved in ethanol and reduced with hydrogen gas on a Parr apparatus using palladium on charcoal as the catalyst. The white solid product is recrystallized from benzene to provide 2,6-di(t-butyl)-4-(2'-methoxyphenyl)phenol, m.p. 98.5°-100° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04232043 |
| 出典データセット | uspto-grants-1980_11 |
| ORD ID | ord-e771728020d14ec48bcbb174f464430d |
| 出典メモ | uspto-grants-1980_11 |