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Acetone → 2H-1-Benzopyran-2,6-diol, 3,4-dihydro-2,5,7,8-tetramethyl-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetone | HCID 180 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Trimethylhydroquinone | HCID 12785 | — |
| 反応物 | 2H-1-Benzopyran-6-ol, 3,4-dihydro-2-methoxy-2,5,7,8-tetramethyl- | HCID 103763 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2H-1-Benzopyran-2,6-diol, 3,4-dihydro-2,5,7,8-tetramethyl- | HCID 103737 | — |
反応手順
A solution of (±)-6-hydroxy-2-methoxy-2,5,7,8-tetramethylchroman, prepared as described in Example 1 from 1.0 mole of trimethylhydroquinone, in 1250 ml. of acetone, 1000 ml. of H2O and 8.30 ml. of conc. HCl was heated at reflux under N2. The solvent was removed by distillation until the distilling head temperature reached 95°. The suspension was cooled to 70°, diluted with 800 ml. of acetone, cooled to ca. 15° and stripped of solvent at reduced pressure and 30° to ca. 1000 ml. The resulting suspension was cooled, filtered and dried to give (±)-2,6-dihydroxy-2,5,7,8-tetramethylchroman as a grey-tan powder, m.p. 105°-107°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04018799 |
| 出典データセット | uspto-grants-1977_04 |
| ORD ID | ord-965226737cd048c796b6ab77ecae8c92 |
| 出典メモ | uspto-grants-1977_04 |