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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1,4-Diisocyanatobenzene | HCID 61009 | — |
| 반응물 | Ethyl 3-(2-chlorophenyl)prop-2-ynoate | HCID 641308 | — |
| 반응물 | 2-(2-Nitroethoxy)tetrahydropyran | HCID 3748656 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 5-(2-Chloro-phenyl)-3-(tetrahydro-pyran-2-yloxymethyl)-isoxazole-4-carboxylic acid ethyl ester | HCID 69123621 | 94.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07179804B2 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-341fc749cbda49a795d8b7d91d739698 |
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| 출처 메모 | uspto-grants-2007_02 |
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