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p-Toluenesulfonic acid → 2-(2-Benzyloxyethoxy)-cyclohexanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Cyclohexanone, 2-hydroxy- | HCID 10785 | — |
| 反応物 | 2-(Benzyloxy) ethanol | HCID 12141 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 2-(2-Benzyloxyethoxy)-cyclohexanone | HCID 20077960 | 67.1% |
反応手順
A mixture of dimeric 2-hydroxycyclohexanone (13.7 g), 2-benzyloxyethanol (20 g) and p-toluensulphonic acid (2 g) were dissolved in xylene (500 ml) in a round bottom flask fitted with a Dean Stark apparatus and reluxed for 10 hrs. The resulting solution was cooled, washed with sodium hydrogen carbonate (3×50 ml) dried and concentrated under reduced pressure. The crude oil was then pruified by flash chromatography using cyclohexane/ethyl acetate 60/40 as eluant yielding 20 g of the title compound (RF=0.5).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05138048 |
| 出典データセット | uspto-grants-1992_08 |
| ORD ID | ord-1e72999ae0a440dd8c452fa2cf8d058f |
| 出典メモ | uspto-grants-1992_08 |