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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905055생성일: 2026년 10월 26일

2,4-Dichlorobenzyl alcohol → trans-6-(2,4-Dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyran

https://huagongshe.com/reaction/905055

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dichlorobenzyl alcoholHCID 15684—
반응물(3,4-dihydro-2H-pyran-2-yl)methyl 4-methylbenzene-1-sulfonateHCID 13071283—
촉매TriethylamineHCID 8471—
촉매Phosphorus oxychlorideHCID 24813—
용매Diethyl EtherHCID 3283—
생성물trans-6-(2,4-Dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyranHCID 1307391681.8%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04421758
출처 데이터셋uspto-grants-1983_12
ORD IDord-963b87fab3af4ff0bf5eb899ec0cab23
출처 메모uspto-grants-1983_12