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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18169생성일: 2026년 10월 25일

Hydrochloric Acid → 4-Fluoro-2-hydroxybenzaldehyde

https://huagongshe.com/reaction/18169

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물TriethylamineHCID 8471—
반응물3-FluorophenolHCID 9743—
반응물HCID 178418443HCID 178418443—
용매BenzeneHCID 241—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-Fluoro-2-hydroxybenzaldehydeHCID 277926836.3%

반응 단계

To a solution of 3-fluorophenol (1 ml, 11 mmol) in THF (20 ml) in a three-neck flask was added ethylmagnesium bromide (5.5 ml, 5.5 mmol, 1M in THF). After stirring at room temperature for 2 hours, benzene was added to the reaction mixture and THF was removed by distillation at 80° C. Additional benzene (50 ml) was added to the reaction, followed by NEt3 (2.3 ml, 16.5 mmol) and paraformaldehyde (1 g, 33.3 mmol). After heating at reflux for 3 hours, the reaction mixture was allowed to cool to room temperature and was poured into 250 ml of 10% HCl. EtOAc was added and the organic layer was separated and washed with H2O. After drying over MgSO4, the solvent was removed under reduced pressure. The resulting residue was purified by flash chromatography to give 4-fluoro-2-hydroxy-benzaldehyde as a white solid (560 mg, 36%), 1H NMR (CDCl3, 300 MHz) δ: 6.71 (m, 2H), 7.56 (dd, 1H, J=6.3 Hz, 8.6 Hz), 9.84 (s, 1H), 11.36 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741326B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-181d57e23e8f4d86b4e5d685e0a7fe14
출처 메모uspto-grants-2010_06