돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 442928생성일: 2026년 10월 24일

1,3-Propanediol → 3-[3-(2-Cyanophenylsulfonyloxy)-5-methylphenoxy]propanol

https://huagongshe.com/ko/reaction/442928

반응식

참여 물질

역할이름HCID투입량
반응물1,3-PropanediolHCID 10442—
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물3-(2-Cyanophenylsulfonyloxy)-5-methylphenolHCID 22722643—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물3-[3-(2-Cyanophenylsulfonyloxy)-5-methylphenoxy]propanolHCID 1866970680.6%

반응 단계

To a solution of 3-(2-cyanophenylsulfonyloxy)-5-methylphenol (580 mg, 2.0 mmol), as prepared in the preceding step, tri-n-butylphosphine (607 mg, 3.0 mmol), and 1,3-propanediol (760 mg, 10 mmol) in anhydrous tetrahydrofuran (20 mL) was added 1,1'-(azodicarbonyl)dipiperidine (757 mg, 3.0 mmol). The mixture was stirred at room temperature overnight. Hexane (30 mL) was added to the mixture, and the precipitates were removed by filtration. The filtrate was evaporated in vacuo, and the residue was purified by flash column chromatography (10% ethyl acetate in dichloromethane) to give the title compound as a colorless oil (560 mg, 80%). 1H-NMR (300 MHz, CDCl3) δ 8.11 (m, 1H), 7.94 (m, 1H), 7.77-7.82 (m, 2H), 6.65 (s, 1H), 6.59 (s, 1H), 6.57 (s, 1H), 4.05 (t, J=6.0 Hz, 2H), 3.82 (t, J=6.0 Hz, 2H), 2.26 (s, 3H), 2.00 (m, 2H), 1.76 (brs, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05891909
출처 데이터셋uspto-grants-1999_04
ORD IDord-6a7299b0985b444e878cb3974601c996
출처 메모uspto-grants-1999_04