돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 545081생성일: 2026년 10월 27일

Trifluoroacetic anhydride → 2-Chloro-5-(trifluoromethyl)pyridine 1-oxide

https://huagongshe.com/reaction/545081

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic anhydrideHCID 9845—
반응물Carbamide PeroxideHCID 31294—
반응물2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
용매DichloromethaneHCID 6344—
생성물2-Chloro-5-(trifluoromethyl)pyridine 1-oxideHCID 15448342—

반응 단계

Cool a DCM (500 mL) solution of 2-chloro-5-trifluoromethylpyridine (96 g, 529 mmol) to 0° C. in an ice bath. Add urea hydrogen peroxide (105 g, 1111 mmol), followed by dropwise addition of trifluoroacetic anhydride (147 mL, 1058 mmol), and allow the reaction mixture to reach room temperature. After 22 hours, TLC (50% EtOAc/Hexanes) shows only a trace amount of starting material. Quench the reaction with sat. aqueous Na2S2O3 and stir for 15 minutes to destroy any residual peroxides. Then, pour the mixture into 0.5 M HCl (300 mL) and extract with CH2Cl2 (2×200 mL). Wash the combined organic extracts with sat. NaHCO3 (3×100 mL), dry over Na2SO4, filter, and concentrate under vacuum to give the title product as a pale yellow solid, which is used in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 8.60 (s, 1H), 7.64 (d, 1H, J=8.4 Hz), 7.38 (d, 1H, J=8.0 Hz). Mass spec. (481.11, M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07935702B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-357fea5ad95142ca9c170521a7646c1d
출처 메모uspto-grants-2011_05