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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10475생성일: 2026년 10월 24일

2-Methylbenzenesulfonic acid → 2H-Pyran, tetrahydro-2-(4-iodophenoxy)-

https://huagongshe.com/ko/reaction/10475

반응식

참여 물질

역할이름HCID투입량
반응물2-Methylbenzenesulfonic acidHCID 6925—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물4-IodophenolHCID 10894—
촉매p-Toluenesulfonic acidHCID 6101—
용매DichloromethaneHCID 6344—
생성물2H-Pyran, tetrahydro-2-(4-iodophenoxy)-HCID 291680392.1%

반응 조건

온도20 °C

반응 단계

To a stirred solution of 4-iodophenol (11.0 g, 50 mmol) in CH2Cl2 (50 ml) cooled with an ice bath, dihydropyran (5.0 g, 60 mmol) was added dropwise over 10 min at 0–5° C. After the solution became clear, toluenesulfonic acid, TsOH, (10 mg) was added. The solution was stirred at 20° C. for 15 min. Then it was quenched by addition of NaHCO3 (1 g) and 3 drops of water, and after stirring for 5 min at 20° C., the solvent was removed in vacuo and the residue was purified by column chromatography on silica gel with petroleum ether as eluent to give 14.0 g (92%) of 1 as colorless crystal; mp 66° C.; δH(CDCl3; 300 MHz): 7.55(d, J=8.3, 2H, Ar—H), 6.83(d, J=8.4, 2H, Ar—H), 5.37(t, J=3.1, 1H, OCHO), 3.86(m, 1H, THP), 3.59(m, 1H, THP), 1.87˜1.58(m, 6H, THP).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094809B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-1bb450c743ff480295cb2836392ef9e4
출처 메모uspto-grants-2006_08