関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| 反応物 | 1-(4-Bromophenyl)ethanol | HCID 95352 | — |
| 触媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-(p-Bromo-alpha-methylbenzyloxy)tetrahydropyran | HCID 11219861 | — |
反応手順
A mixture of 269 parts of p-bromo-α-methylbenzyl alcohol and 225 parts of 2H-3,4-dihydropyran is stirred and cooled to 0° C. Then there are added dropwise 10 drops of concentrated hydrochloric acid solution and the whole is stirred in an ice-bath (room temperature is reached). After stirring for 24 hours, the reaction mixture is poured onto 1200 parts of ether. The organic phase is washed twice with a sodium hydrogen carbonate solution and twice with water, dried, filtered and evaporated. The residue is distilled, yielding 2-(p-bromo-α-methylbenzyloxy)tetrahydropyran; bp. 165°-177° C. at 20 mm. pressure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04035376 |
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| 出典データセット | uspto-grants-1977_07 |
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| ORD ID | ord-7de4891e22fe41ca84d1bd5bba4b0925 |
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| 出典メモ | uspto-grants-1977_07 |
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