Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2,4-Dichlorobenzyl alcohol → trans-6-(2,4-Dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyran
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2,4-Dichlorobenzyl alcohol | HCID 15684 | — |
| 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-(2,4-Dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyran | HCID 13073916 | 81.8% |
반응 단계
To a solution of 1.34 g of 2-tosyloxymethyl-3,4-dihydro-2H-pyran in 25 ml of diethyl ether were added 1.06 g of 2,4-dichlorobenzyl alcohol, followed by a catalytic amount (2-3 drops) of phosphorus oxytrichloride. The mixture was then stirred at room temperature for 4 days, after which 3 drops of triethylamine were added to the mixture, which was then concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel as in Example 1(a), to give 1.82 g of trans-6-(2,4-dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyran (having the lesser polarity), 144 mg of cis-6-(2,4-dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyran (having the greater polarity) and 200 mg of a cis/trans mixture.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04421758 |
| 출처 데이터셋 | uspto-grants-1983_12 |
| ORD ID | ord-963b87fab3af4ff0bf5eb899ec0cab23 |
| 출처 메모 | uspto-grants-1983_12 |