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4-Hydroxybenzyl Alcohol → 4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)phenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Hydroxybenzyl Alcohol | HCID 125 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 3-Tert-butyl-4-methoxybenzoyl chloride | HCID 13633555 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)phenol | HCID 21474530 | — |
反応手順
1.24 g (0.01 mol) of 4-hydroxybenzenemethanol, 1 ml (0.01 mol) of pyridine and 50 ml of THF are introduced into a round-bottomed flask. While cooling in an icebath, a solution of 2.2 g (0.01 mol) of 3-tert-butyl-4-methoxybenzoyl chloride in 50 ml of THF is introduced dropwise and the mixture is stirred at room temperature for 24 h. The reaction medium is poured into water, the mixture is extracted with ethyl ether and the organic phase is separated after settling has taken place, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column and eluted with a mixture of dichloromethane and ethyl ether (97:3).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05387594 |
| 出典データセット | uspto-grants-1995_02 |
| ORD ID | ord-6f43e7ba229e4366a2732b9a84ac901f |
| 出典メモ | uspto-grants-1995_02 |