참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| 반응물 | 1-(4-Bromophenyl)ethanol | HCID 95352 | — |
| 촉매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 2-(p-Bromo-alpha-methylbenzyloxy)tetrahydropyran | HCID 11219861 | — |
반응 단계
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; b.p. 165°-177° C. at 20 mm. pressure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04064132 |
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| 출처 데이터셋 | uspto-grants-1977_12 |
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| ORD ID | ord-fbaac15cfa1841cd91d91940aa02c778 |
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| 출처 메모 | uspto-grants-1977_12 |
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