Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid → 1-Benzyloxy-4-(2-tetrahydropyran-2-yloxyethyl)benzene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| 반응물 | p-(Benzyloxy)phenethyl alcohol | HCID 3017260 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-Benzyloxy-4-(2-tetrahydropyran-2-yloxyethyl)benzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04761420 |
| 출처 데이터셋 | uspto-grants-1988_08 |
| ORD ID | ord-f92efd1f6d3f4d53b725d2188aaf8482 |
| 출처 메모 | uspto-grants-1988_08 |