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Potassium Hydroxide → 4-tert-Butylphenylacetylene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | ((4-(tert-Butyl)phenyl)ethynyl)trimethylsilane | HCID 14989664 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 4-tert-Butylphenylacetylene | HCID 2757302 | — |
反応手順
To a stirred solution of 1.44 g (6.23 mmol) of trimethylsilyl (4-tert-butyl) phenylethyne (Compound 21) in 5 ml of isopropanol was added 10 ml of 1N aqueous KOH and the mixture then stirred at room temperature for 6.5 hours. The isopropanol was removed under vacuum and the residue extracted with ether. The ether extract was washed with dilute HCl until the washings were acidic. The ether solution was then successively washed with water, saturated NaCl and NaHCO3 solutions and then dried (MGSO4). Solvent was then removed in-vacuo to give the title compound as a colorless oil. PMR (CDCl3): & 1.34 (9H, s), 3.05 (1H, s), 7.37 (2H, d, J~8.2 Hz), 7.46 (2H, d, J~8.2 Hz).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05264456 |
| 出典データセット | uspto-grants-1993_11 |
| ORD ID | ord-90a288469f7a47ab98bb7b39d840b463 |
| 出典メモ | uspto-grants-1993_11 |