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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34406생성일: 2026년 10월 26일

p-Toluenesulfonic acid → 1-Benzyloxy-4-(2-tetrahydropyran-2-yloxyethyl)benzene

https://huagongshe.com/reaction/34406

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물p-(Benzyloxy)phenethyl alcoholHCID 3017260—
용매DichloromethaneHCID 6344—
생성물1-Benzyloxy-4-(2-tetrahydropyran-2-yloxyethyl)benzeneHCID 14208782—

반응 단계

To a solution of 1-benzyloxy-4-(2-hydroxyethyl)benzene (7, 20 g, 87.7 mmoles) in CH2Cl2 (175 mL) was added 4-toluenesulfonic acid (TsOH, 0.17 g, 0.9 mmoles) and dihydropyran (9.9 mL dropwise, 108 mmoles). The mixture was stirred for 4 h and the solvent evaporated under reduced pressure to yield 28 g of crude product. This was purified by flash chromatography (solvent=70:30 ethyl acetate:heptane). The pure fractions were pooled and the solvent evaporated to give 1-benzyloxy-4-(2-tetrahydropyran-2-yloxyethyl)benzene (8, 26.5 g). NMR (CDCl3)δppm: 7.30(s, 5H); 6.97(q, 4H); 4.95(s, 2H); 7.87(s, 1H); 4.2-3.4(m, 4H); 2.8(t, 2H); 1.9-1.3(m, 6H). (Scheme II, Step 3.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04761420
출처 데이터셋uspto-grants-1988_08
ORD IDord-f92efd1f6d3f4d53b725d2188aaf8482
출처 메모uspto-grants-1988_08