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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1712432생성일: 2026년 10월 25일

3,4-dihydro-2H-pyran → 2-(4-Methyl-3-nitrobenzyloxy)tetrahydropyran

https://huagongshe.com/reaction/1712432

반응식

참여 물질

역할이름HCID투입량
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물4-Methyl-3-nitrobenzyl alcoholHCID 123497—
반응물Sodium BicarbonateHCID 516892—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
용매DichloromethaneHCID 6344—
생성물2-(4-Methyl-3-nitrobenzyloxy)tetrahydropyranHCID 68503488—

반응 단계

The solution of 9.85 g of 4-methyl-3-nitrobenzyl alcohol in 200 ml of dichloromethane is admixed successively with 10.9 ml of 3,4-dihydro-2H-pyran and 1.12 g of p-toluenesulphonic acid monohydrate. The reaction mixture is stirred at room temperature over 18 hours. The solution is poured onto 1M sodium hydrogencarbonate solution (300 ml) and extracted with tert-butyl methyl ether (2×300 ml). The organic phase is washed with brine (300 ml), dried over sodium sulphate, filtered and concentrated by evaporation. The title compound is obtained as a colourless oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.49 (1:2 EtOAc-heptane); Rt=4.73.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790715B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-6689eb5700c143e7b2d2ba876daf3a32
출처 메모uspto-grants-2010_09