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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 603113생성일: 2026년 10월 25일

Hydrochloric Acid → 4-(1-Cyanocyclobutyl)benzonitrile

https://huagongshe.com/reaction/603113

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-FluorobenzonitrileHCID 14517—
반응물CyanocyclobutaneHCID 78148—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
용매TetrahydrofuranHCID 8028—
생성물4-(1-Cyanocyclobutyl)benzonitrileHCID 5829848755.3%

반응 조건

온도0 °C

반응 단계

Solid KHMDS (3.48 g, 17.5 mmol) is dissolved in THF (20.0 mL) and cooled to 0° C. Cyclobutanecarbonitrile (1.42 g, 17.5 mmol) is added, and the resulting solution stirred for 40 minutes. A solution of 4-fluorobenzonitrile (2.12 g, 17.5 mmol) in THF (10.0 mL) is added, and the mixture stirred for 2 hours at 0° C. 1N HCl (50.0 mL) is added to the reaction mixture and the aqueous phase extracted with EtOAc (4×40.0 mL). The combined organic phases are dried over MgSO4, filtered and concentrated on the rotovaporator. The product is purified by flash chromatography (CombiFlash), eluting with mixtures of heptanes and EtOAc (0% EtOAc to 40% EtOAc) to yield the desired product (1.76 g, 9.67 mmol, 55%). 1H NMR (400 MHz, DMSO-D6) ε ppm 1.92-2.12 (m, 1H) 2.19-2.37 (m, 1H) 2.57-2.69 (m, 2H) 2.71-2.82 (m, 2H) 7.67 (d, J=8.59 Hz, 2H) 7.91 (d, J=8.79 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906654B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-84ebabcd9ce14158bac68c778d9469e3
출처 메모uspto-grants-2011_03