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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 930642생성일: 2026년 10월 24일

Acetic Anhydride → 4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-one

https://huagongshe.com/ko/reaction/930642

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물4-(4-(Trifluoromethyl)benzyloxy)pyridine 1-oxideHCID 68657649—
생성물4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-oneHCID 5795048091%

반응 조건

온도80 °C

반응 단계

4-(4-(Trifluoromethyl)benzyloxy)pyridine 1-oxide (600 mg, 2.22 mmol) was heated to 140° C. in acetic anhydride (20 mL) for 2 h. The mixture was concentrated and then heated at 80° C. for 1 h in a mixture of MeOH (10 mL) and aqueous 1 N NaOH (10 mL). The resultant black solution was concentrated to a volume of 10 mL and extracted with CHCl3/EtOH (3:1). The organic layer was removed and concentrated to provide the title compound (550 mg, 91%) as a tan solid: 1H NMR (300 MHz, CD3OD) δ 7.70-7.60 (m, 4H), 7.41 (d, J=7.0 Hz, 1H), 6.17 (dd, J=7.0, 2.5 Hz, 1H), 5.96 (d, J=2.4 Hz, 1H), 5.18 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09296743B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-0c740a6f9da54177bb895d4fbbff3e89
출처 메모uspto-grants-2016_03