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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1492371생성일: 2026년 10월 25일

3-(Trifluoromethyl)phenol → 2-(3-Trifluoromethylphenoxy)-6-benzyloxypyridine

https://huagongshe.com/reaction/1492371

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)phenolHCID 7376—
반응물2-(Benzyloxy)-6-chloropyridineHCID 11264464—
용매DimethylformamideHCID 6228—
용매Sodium hydrideHCID 24758—
생성물2-(3-Trifluoromethylphenoxy)-6-benzyloxypyridineHCID 2147106378.8%

반응 단계

The procedure of Example 4a) was also used to introduce the 3-trifluoromethyl phenoxy group by reaction of 2-benzyloxy-6-chloropyridine (5 g; 23 mmols) from a) above with 3-trifluoromethylphenol (3.3 g; 0.018 mols) using dry sodium hydride (0.55 g) and dry dimethylformamide (200 ml) as solvent, with a 1 hour reflux stage. 2-(3-Trifluoromethylphenoxy)-6-benzyloxypyridine (4.9 g; 51%) was obtained as a yellow oil following solvent extraction (chloroform/water--500 ml; 50/50), and chromatography plus distillation of the organic layer.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05374604
출처 데이터셋uspto-grants-1994_12
ORD IDord-9e8aa03260f841788284981f9f77c884
출처 메모uspto-grants-1994_12