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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2108711생성일: 2026년 10월 26일

Hydrochloric Acid → 2-Fluorobenzofuran-5-carbaldehyde

https://huagongshe.com/reaction/2108711

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물TetrahydrofuranHCID 8028—
반응물MagnesiumHCID 5462224—
반응물5-Bromo-2-fluoro-1-benzofuranHCID 57439113—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물2-Fluorobenzofuran-5-carbaldehydeHCID 45090831—

반응 단계

A slurry of magnesium powder (219 mg) and iodine (cat) in dry tetrahydrofuran (3 ml) was heated at 50° C. under nitrogen for 20 minutes. 5-Bromo-2-fluoro-1-benzofuran (1.4 g) was dissolved in dry tetrahydrofuran (6 ml). A 1 ml portion of the solution was added to the slurry at 50° C. without stirring. After 30 minutes the rest of the solution was added slowly and the reaction was heated at reflux for 3 hours. The reaction was cooled in an ice/water bath and dimethylformamide (1 ml) was added dropwise maintaining the temperature below 10° C. After 1 hour a mixture of 2N hydrochloric acid (12.5 ml) and brine (12.5 ml) was added. The reaction mixture was extracted using ethyl acetate (3×25 ml). The combined organics were washed with brine and dried over anhydrous magnesium sulphate. The solvent was removed in vacuo and the residue applied to a silica cartridge (50 g). This was eluted with cyclohexane, cyclohexane/ethyl acetate (6:1, 5:1 v/v). This gave 2-fluoro-5-formyl-1-benzofuran (376 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07514437B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-53849f3ae6794609b1e0232446cc8194
출처 메모uspto-grants-2009_04