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Diethyl Ether → 2-(6-Chlorohexyloxy)tetrahydro-2H-pyran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| 反応物 | 6-Chloro-1-hexanol | HCID 74828 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 触媒 | p-Toluenesulfonic acid | HCID 6101 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(6-Chlorohexyloxy)tetrahydro-2H-pyran | HCID 329803 | 86.6% |
反応手順
To a mixture of 15 g of 6-chlorohexanol, 100 ml of methylenechloride and 0.2 g of p-toluenesulphonic acid were added dropwise 12 g of dihydropyrane in 40 ml of methylenechloride. The reaction mixture was stirred for 15 h at room temperature and then distributed between ether and saturated sodium bicarbonate solution. The ether phase was washed with water, dried over sodium sulphate, filtered and concentrated to dryness. Chromatography of the residue on silica using hexane/ether (3:1) gave 21 g of the product as a colourless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07419620B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-a770b83f1db64c9a9292a5aa6bd5ee65 |
| 出典メモ | uspto-grants-2008_09 |