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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905062생성일: 2026년 10월 26일

(3,4-dihydro-2H-pyran-2-yl)methyl 4-methylbenzene-1-sulfonate → Trans-6-[alpha-(4-chlorophenyl)-2,4-dichlorobenzyloxy]-2-tosyloxymethyltetrahydropyran

https://huagongshe.com/reaction/905062

반응식

참여 물질

역할이름HCID투입량
반응물(3,4-dihydro-2H-pyran-2-yl)methyl 4-methylbenzene-1-sulfonateHCID 13071283—
반응물2,4,4'-TrichlorobenzhydrolHCID 22565435—
촉매TriethylamineHCID 8471—
촉매Phosphorus oxychlorideHCID 24813—
생성물Trans-6-[alpha-(4-chlorophenyl)-2,4-dichlorobenzyloxy]-2-tosyloxymethyltetrahydropyranHCID 53867744—

반응 단계

2.10 g of α-(4-chlorophenyl)-2,4-dichlorobenzyl alcohol and 1.78 of 2-tosyloxymethyl-3,4-dihydro-2H-pyran were dissolved in 40 ml of diethyl ester, and a catalytic amount (2 drops) of phosphorus oxytrichloride was added to the solution. The mixture was then stirred at room temperature for 4 days, after which 3 drops of triethylamine were added. The mixture was then concentrated by evaporation under reduced pressure and the residue was purified by column chromatography through silica gel eluted with a 15:5:1 by volume mixture of hexane, benzene and ethyl acetate, to give 3.41 g of the title compound in the form of a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04421758
출처 데이터셋uspto-grants-1983_12
ORD IDord-b6aa40c21ef24b06a2d1e5d660883ff9
출처 메모uspto-grants-1983_12