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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349260생성일: 2026년 10월 26일

Triethylamine → 5-(2-Chloro-phenyl)-3-(tetrahydro-pyran-2-yloxymethyl)-isoxazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/349260

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,4-DiisocyanatobenzeneHCID 61009—
반응물Ethyl 3-(2-chlorophenyl)prop-2-ynoateHCID 641308—
반응물2-(2-Nitroethoxy)tetrahydropyranHCID 3748656—
용매TolueneHCID 1140—
생성물5-(2-Chloro-phenyl)-3-(tetrahydro-pyran-2-yloxymethyl)-isoxazole-4-carboxylic acid ethyl esterHCID 6912362194.2%

반응 조건

온도70 °C

반응 단계

Add 2-(2-nitroethoxy)tetrahydropyran (41 mL, 270 mmol) dropwise in toluene (100 mL) to a solution of (2-chloro-phenyl)-propynoic acid ethyl ester (28.3 g, 135 mmol), 1,4-phenylene diisocyanate (67 g, 420 mmol) and triethylamine (15 mL) in toluene (900 mL). Stir at reflux for 10 h. While still warm (˜70° C.), filter the reaction mixture through Celite®, washing the solids with EtOAc. Wash the filtrate with 1N HCl (500 mL) and brine (500 mL). Dry the organics over Na2SO4, filter and concentrate under reduced pressure. Purification by flash chromatography (silica gel, 85:15 Hexanes/EtOAc) gives the title compound (46.5 g, 94%). MS (m/e): 282 (M−C5H8O+H+); 1H NMR (300 MHz, CDCl3) δ 7.35–7.55 (m, 4H), 5.09 (d, J=13 Hz, 1), 4.85–4.91 (m, 2H), 4.15–4.22 (m, 2H), 3.91–4.01 (m, 1H), 3.52–3.61 (m, 1H), 1.49–1.92 (m, 6H), 1.12 (t, J=7 Hz, 3H); TLC Rf=0.53 (7:3 Hexanes/EtOAc).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179804B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-341fc749cbda49a795d8b7d91d739698
출처 메모uspto-grants-2007_02