참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Chlorobenzyl alcohol | HCID 13397 | — |
| 반응물 | (3,4-dihydro-2H-pyran-2-yl)methyl 4-methylbenzene-1-sulfonate | HCID 13071283 | — |
| 촉매 | Triethylamine | HCID 8471 | — |
| 촉매 | Phosphorus oxychloride | HCID 24813 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | trans-6-(4-Chlorobenzyloxy)-2-tosyloxymethyltetrahydropyran | HCID 13261931 | 74.9% |
반응 단계
3 g of 2-tosyloxymethyl-3,4-dihydro-2H-pyran and 1.91 g of p-chlorobenzyl alcohol were dissolved in 40 ml of diethyl ether, and 2-3 drops of phosphorus oxytrichloride were added to the resulting solution. The mixture was then allowed to react at room temperature for 1.5 days, after which 2 drops of triethylamine were added and the mixture was concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through silica gel, eluted with a 8:1 by volume mixture of hexane and ethyl acetate, to give 3.44 g of trans-6-(4-chlorobenzyloxy)-2-tosyloxymethyltetrahydropyran (having the lesser polarity), 0.59 g of cis-6-(4-chlorobenzyloxy)-2-tosyloxymethyltetrahydropyran (having the greater polarity) and 0.86 g of an approximately 1:1 cis/trans mixture.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04421758 |
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| 출처 데이터셋 | uspto-grants-1983_12 |
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| ORD ID | ord-10a4d67faeae4178a03af7919c790598 |
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| 출처 메모 | uspto-grants-1983_12 |
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