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Butylate → 7-Methoxy-1-vinylnaphthalene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Butylate | HCID 16181 | — |
| 反応物 | Potassium | HCID 5462222 | — |
| 反応物 | 2-(7-Methoxynaphthalen-1-yl)ethyl methanesulfonate | HCID 19085990 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 7-Methoxy-1-vinylnaphthalene | HCID 44541668 | — |
反応手順
The compound obtained in Step A (21.4 mmol) is dissolved in 120 ml of tetrahydrofuran, and potassium tent-butylate (64.2 mmol) is added in small portions. After stirring for 30 minutes at ambient temperature, the reaction mixture is evaporated to dryness. The residue obtained is taken up in 150 ml of water and the aqueous phase is extracted twice with 60 ml of diethyl ether. The organic phase is washed with water, dried over magnesium sulphate, decolourised on vegetable carbon and evaporated. The residue obtained is purified on silica gel (eluant: petroleum ether) to yield the title product in the form of a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07947852B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-c307d8c7baac4019b1c29cce6b41bdff |
| 出典メモ | uspto-grants-2011_05 |