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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50112생성일: 2026년 10월 24일

Hydrochloric Acid → 4-Biphenylcarboxylic acid, 4'-chloro-

https://huagongshe.com/ko/reaction/50112

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium BicarbonateHCID 516892—
반응물4'-Chloro[1,1'-biphenyl]-4-carbaldehydeHCID 592570—
반응물Sodium BisulfiteHCID 23665763—
반응물Potassium hydroxy sulfiteHCID 23707502—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Chloroform methanolHCID 21584188—
용매Acetone acetonitrileHCID 21918305—
생성물4-Biphenylcarboxylic acid, 4'-chloro-HCID 616002—

반응 단계

To a stirred solution of 4-(4-chlorophenyl)benzaldehyde (0.84 g, 3.9 mmol) in 30 mL acetonitrile-acetone (2: 1) is added 15 mL water and solid sodium bicarbonate (3.5 g, 41.7 mmol). After 5 min. a 25 mL solution of oxidation reagent (Oxone: 4.8 g, 7.8 mmol in 25 mL water containing 4×10−4 M EDTA) is added dropwise over 15 min. then stirred for an additional 3.5 h. The reaction mixture is then treated with 18 mL aq. sodium bisulfite (9.5 g), stirred 2 h, then acidified with 10 mL 6 M HCl. The mixture is transferred to a separatory funnel and diluted with 300 mL dichloromethane and 400 mL water. The water layer is washed with dichloromethane (3×120 mL), organic layers combined, then washed with 500 mL water. The organic layer is dried over sodium sulfate, filtered, and evaporated under reduced pressure. The desired acid is crystallized from acetone-water (5:2), filtered, washed with water, and evaporated under reduced pressure from toluene affording 0.6 g product. Remaining product could be isolated by chromatography but the amount obtained is satisfactory. TLC: Rf=0.3 (chloroform-methanol; 10:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710168B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-3a8c1690f10045109a2eb24e686d2372
출처 메모uspto-grants-2004_03