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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1358784생성일: 2026년 10월 26일

Ethanol, 1-ethoxy-2,2,2-trifluoro- → 4-chloro-N-(2,2,2-trifluoro-1-hydroxyethyl)benzamide

https://huagongshe.com/reaction/1358784

반응식

참여 물질

역할이름HCID투입량
반응물Ethanol, 1-ethoxy-2,2,2-trifluoro-HCID 9897—
반응물4-ChlorobenzamideHCID 12084—
반응물Sodium SulfateHCID 24436—
용매1,4-DioxaneHCID 31275—
생성물4-chloro-N-(2,2,2-trifluoro-1-hydroxyethyl)benzamideHCID 11322758—

반응 단계

A solution of 4-chlorobenzamide (22.0 g, 0.141 mol) and trifluoroacetaldehyde ethyl hemiacetal (25.0 g as is, 22.5 g real, 0.156 mol) in dioxane (200 mL) is treated with anhydrous sodium sulfate (10 g, to dry the 10% water in the hemiacetal) and refluxed for 60 hours. The solids are filtered and the filtrate is evaporated to a solid. The solids are dissolved in about 200 mL of 15% ethyl acetate in heptane. Unreacted starting material (5.6 g) crystallizes out and is filtered. The title product is obtained from the mother liquors as a white crystalline solid (22.1 g, 82.9% based on recovery of starting material): mp 139.5-140.5° C.; characterized by 1H and 19F NMR and Mass spectra. 1H NMR (DMSO-d6) δ9.45 (d, J=8.7 Hz, NH), 7.93, 7.54 (AB with fine splitting, J=8.4 Hz, ArH), 7.54 (broad s, OH), 5.90 (m, J=8.7, 2.9, 5.8 Hz, CH); 19F NMR δ−80.3 (d, J=5 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06596902B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-f28b91eb54054a85913918398751affb
출처 메모uspto-grants-2003_07