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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21351생성일: 2026년 10월 26일

Benzoic Acid → 3-Fluoro-4-methoxybenzoic acid

https://huagongshe.com/reaction/21351

반응식

참여 물질

역할이름HCID투입량
반응물Benzoic AcidHCID 243—
반응물Sodium HydroxideHCID 14798—
반응물BromineHCID 24408—
반응물1-(3-Fluoro-4-methoxyphenyl)ethan-1-oneHCID 96828—
반응물SodiumHCID 5360545—
반응물sodium hypobromiteHCID 178507097—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물3-Fluoro-4-methoxybenzoic acidHCID 2733401—
생성물sodium hypobromiteHCID 178507097—

반응 단계

3-fluoro-4-methoxyacetophenone (11.5 g) was dissolved in 100 ml dioxane and NaOBr solution (as prepared below) was added dropwise, with constant stirring with a stir bar at room temperature. The NaOBr solution was prepared by dissolving 40 g of NaOH in 500 ml of water, cooling to 0° C. in an ice bath, and adding bromine (12.5 ml) dropwise while stirring with stir bar; bromine was added slowly so that the reaction mixture did not exceed 5° C. After overnight stirring of the 3-fluoro-4-methoxyacetophenone, dioxane and NaOBr solution, the reaction mixture was diluted with water (200 ml). Since the reaction mixture was basic, the product, benzoic acid, was in water as its sodium salt. The resultant mixture was partitioned between ether and water. The ether layer was washed with dilute aqueous NaOH to extract any remaining product as Na salt. The aqueous layers were combined and acidified to pH 1 to precipitate the benzoic acid. The resulting acid was extracted with ether. The ether layer was washed with water a few times, dried with MgSO4, and filtered. Rotary evaporation of the ether fraction afforded 3-fluoro-4-methoxybenzoic acid (IV) in 85% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05422037
출처 데이터셋uspto-grants-1995_06
ORD IDord-93fc24620c104a2c9d3ba2a8256382e3
출처 메모uspto-grants-1995_06