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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905053생성일: 2026년 10월 25일

4-Chlorobenzyl alcohol → trans-6-(4-Chlorobenzyloxy)-2-tosyloxymethyltetrahydropyran

https://huagongshe.com/reaction/905053

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorobenzyl alcoholHCID 13397—
반응물(3,4-dihydro-2H-pyran-2-yl)methyl 4-methylbenzene-1-sulfonateHCID 13071283—
촉매TriethylamineHCID 8471—
촉매Phosphorus oxychlorideHCID 24813—
용매Diethyl EtherHCID 3283—
생성물trans-6-(4-Chlorobenzyloxy)-2-tosyloxymethyltetrahydropyranHCID 1326193174.9%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04421758
출처 데이터셋uspto-grants-1983_12
ORD IDord-10a4d67faeae4178a03af7919c790598
출처 메모uspto-grants-1983_12