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HRID 131332생성일: 2026년 10월 26일

Potassium Phosphate, Tribasic → 2-Amino-5-cyclopropylbenzonitrile

https://huagongshe.com/reaction/131332

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물TricyclohexylphosphineHCID 75806—
반응물2-Amino-5-bromobenzonitrileHCID 429740—
반응물Cyclopropylboronic acidHCID 2760897—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-Amino-5-cyclopropylbenzonitrileHCID 4512219370%

반응 단계

Combine 2-amino-5-bromo-benzonitrile (1.76 g, 8.95 mmol), cyclopropyl boronic acid (1.0 g, 11.64 mmol), tricyclohexylphosphine (0.251 g, 0.89 mmol) and potassium phosphate (6.65 g, 31.26 mmol) in a mixture of toluene (40 ml) and water (2 ml) and stir the mixture for 10 minutes. Add palladium acetate (0.101 g, 0.45 mmol) and heat the mixture to 100° C. After 3 hours add more tricyclohexylphosphine (0.251 g, 0.89 mmol) and palladium acetate (0.101 g, 0.45 mmol). After an additional 3 hours at 100° C., add 20 ml of water and extract the mixture three times with 50 ml of ethyl acetate. Combine the organic layers, dry over sodium sulfate and concentrate. Purify the residue using flash chromatography and eluting with a linear gradient starting with 100% hexanes and going to 70% hexanes: 30% ethyl acetate to obtain 0.988 g of the title compound (6.24 mmol, 70% yield) as a clear yellow oil: Mass spectrum (m/e): 159(M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384934B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-17deea1f29f04740acd3f98d43667bf6
출처 메모uspto-grants-2008_06