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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70583생성일: 2026년 10월 23일

Hydrochloric Acid → HCID 58452334, 화합물

https://huagongshe.com/ko/reaction/70583

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물Triisopropyl borateHCID 21531—
반응물4-Bromo-2-methylbenzonitrileHCID 144267—
반응물ButyllithiumHCID 178418339—
용매HexaneHCID 8058—
생성물HCID 58452334HCID 5845233467%

반응 조건

온도-78 °C

반응 단계

A solution of 4-bromo-2-methylbenzonitrile (1.0 g) in tetrahydrofuran (16 mL) was cooled to an external temperature of −78° C. in a nitrogen atmosphere, and a solution of n-butyllithium in hexane (1.57 M, 3.5 mL) was added dropwise. After stirring at −78° C. for 40 minutes, triisopropyl borate (1.5 mL) was added dropwise and the mixture was stirred at room temperature for 1.5 hours. 1 M hydrochloric acid (10 mL) was added to the reaction solution, followed by extraction with diethyl ether. The organic layer was washed with water and brine, dried over sodium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was dissolved in toluene (4 mL) and tetrahydrofuran (3 mL), and 2,2-dimethyl-1,3-propanediol (531 mg) and anhydrous magnesium sulfate (catalytic amount) were added, after which the mixture was stirred at room temperature for five minutes. The insoluble matter in the reaction solution was filtered off, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=50:1→20:1) to give the title compound as a colorless solid (778 mg, 67%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822503B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f36dc87aec0a48c4ada52f8430ba6537
출처 메모uspto-grants-2014_09