돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1405392생성일: 2026년 10월 26일

Sodium bis(trimethylsilyl)amide → 3-Methyl-4-(oxetan-3-YL)benzonitrile

https://huagongshe.com/reaction/1405392

반응식

참여 물질

역할이름HCID투입량
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물3-IodooxetaneHCID 13356686—
반응물(4-Cyano-2-methyl-phenyl)boronic acidHCID 16218401—
촉매Nickel(II) iodideHCID 26038—
촉매(1S,2S)-2-Aminocyclohexanol hydrochlorideHCID 11715205—
용매EthanolHCID 702—
용매IsopropanolHCID 3776—
생성물3-Methyl-4-(oxetan-3-YL)benzonitrileHCID 6815330965.42%

반응 단계

(4-Cyano-2-methyl-phenyl)boronic acid (1.75 g, 10.87 mmol), diiodonickel (102 mg, 0.326 mmol), (1S,2S)-2-aminocyclohexan-1-ol hydrochloride (50 mg, 0.33 mmol) and NaHMDS (2.01 g, 11.0 mmol) were combined in isopropanol (10 mL) under N2 in a pressure vial. A solution of 3-iodooxetane (1.00 g, 5.44 mmol) in isopropanol (1 mL) was added. The vial was immersed in a pre-heated 90° C. oil bath and stirred for 2 h, then cooled, diluted with ethanol (20 mL), filtered over Celite, concentrated, then absorbed onto Celite and purified by silica gel column chromatography (0-60% EtOAc/hexane) to give 3-methyl-4-(oxetan-3-yl)benzonitrile (616 mg, 3.556 mmol, 65.42%) as a white solid. ESI-MS m/z calc. 173.1, found 174.3 (M+1)+; Retention time: 1.09 minutes (3 min run).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08916565B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-e1140e27dd8b4332a0632d541dab42c0
출처 메모uspto-grants-2014_12