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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218257생성일: 2026년 10월 26일

Hydrochloric Acid → 4-Fluoro-2,3-dihydroxybenzaldehyde

https://huagongshe.com/reaction/218257

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물TriethylamineHCID 8471—
반응물3-FluorocatecholHCID 67764—
반응물Magnesium ChlorideHCID 5360315—
용매AcetonitrileHCID 6342—
용매tert-Butyl methyl etherHCID 15413—
생성물4-Fluoro-2,3-dihydroxybenzaldehydeHCID 4511910319.6%

반응 단계

Magnesium chloride (3.71 g, 33 mmol) was added portionwise at room temperature to a solution of 3-fluorocatechol (2 g, 15.6 mmol) in acetonitrile (20 mL), followed by triethylamine (13.4 mL, 97.5 mmol). Paraformaldehyde (3.16 g, 105.3 mmol) was then added to the stirred suspension and the mixture was heated at reflux for 5 hours. The mixture was cooled to room temperature then poured into a mixture of 5% HCl and TBME. The organic phase was separated, and the aqueous layer re-extracted with TBME. The combined organic extracts were washed with brine, dried over sodium sulphate and the solvent removed under reduced pressure. The crude mixture (˜1:1 starting material:product) was purified on normal silica in neat DCM followed by DCM/MeOH 96:4 and 90:10 to yield 478 mg of 28 still contaminated with 11.4% w/w of 3-fluorocatechol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198302B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-87e79cbc614f479d95cef12d52eb50aa
출처 메모uspto-grants-2012_06