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Epichlorohydrin → 2,2-Dimethyl-4-(naphthalen-1-yl)-7-[(oxiran-2-yl)methoxy]-2H-1-benzopyran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Epichlorohydrin | HCID 7835 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2,2-Dimethyl-4-(naphthalen-1-yl)-2H-1-benzopyran-7-ol | HCID 23330747 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 2,2-Dimethyl-4-(naphthalen-1-yl)-7-[(oxiran-2-yl)methoxy]-2H-1-benzopyran | HCID 23330742 | 86% |
反応手順
2,2-Dimethyl-4-(1-naphthyl)-2H-chromen-7-ol (7.92 g, 0.026 moles) and epichlorohydrin (28,5 ml) were dissolved in acetone (50 ml). Potassium carbonate (6.3 g), was added and the mixture refluxed for 6 hours, allowed to cool and filtered. The acetone was removed in vacuo and the residue dissolved in ether, washed with water and dried. Removal of solvent gave the title product as an orange oil (8.1 g, 86%) which was used in the next reaction without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04234726 |
| 出典データセット | uspto-grants-1980_11 |
| ORD ID | ord-94510f9de2ab43b68c833d135e3ac2f3 |
| 出典メモ | uspto-grants-1980_11 |