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1-Bromopentane → 2-n-Pentoxy-5-nonyl benzophenone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Bromopentane | HCID 8057 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Methanone, (2-hydroxy-5-nonylphenyl)phenyl- | HCID 93939 | — |
| 触媒 | Tetrabutylammonium Bromide | HCID 74236 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-n-Pentoxy-5-nonyl benzophenone | HCID 53893873 | 82% |
反応手順
A solution of 2-hydroxy-5-nonyl benzophenone, 15 g, in 100 mL methylene chloride was mixed with a solution of 9.25 g NaOH in 100 mL water. To this mixture was added 6.9 g n-pentyl bromide and 1.48 g tetra-n-butylammonium bromide. The whole mixture was then vigorously agitated overnight at 40° C. After cooling to room temperature with 50 mL CH2Cl2. The combined methylene chloride layers were concentrated to an oil, which was taken up in 100 mL petroleum ether and washed with 100 mL water. Finally, the organic layer was dried over anhydrous magnesium sulfate and the volatiles removed under vacuum to give 15 g (82% yield) of 2-n-pentoxy-5-nonyl benzophenone.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04578250 |
| 出典データセット | uspto-grants-1986_03 |
| ORD ID | ord-c311d96f2e954f6182650344fbe57b25 |
| 出典メモ | uspto-grants-1986_03 |