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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 449123생성일: 2026년 10월 24일

4-Chlorophenylboronic acid → 2-(4-Chloro-benzyl)-tetrahydropyran

https://huagongshe.com/ko/reaction/449123

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorophenylboronic acidHCID 74299—
반응물2-(Bromomethyl)tetrahydro-2H-pyranHCID 141917—
반응물2-Aminocyclohexanol hydrochlorideHCID 21877202—
반응물Sodium hexamethyidisilazaneHCID 45051731—
촉매Nickel(II) iodideHCID 26038—
용매IsopropanolHCID 3776—
생성물2-(4-Chloro-benzyl)-tetrahydropyranHCID 66915679—

반응 조건

온도60 °C

반응 단계

To a stirred mixture of (4-chlorophenyl)dihydroxyborane (524.0 mg, 3.351 mmol), 2-aminocyclohexanol hydrochloride (42 mg, 0.28 mmol) and nickel iodide (87.3 mg, 0.279 mmol) in i-PrOH (10.00 mL) was added sodium hexamethyldisilazane (1.075 g, 5.864 mmol) at 0° C. Then the mixture was stirred at rt for 5 min before, 2-(bromomethyl)tetrahydro-2-H-pyran (500.00 mg, 2.79 mmol) was added by syringe. The resulting mixture was then stirred at 60° C. for 5 h. The solvent was then removed under reduced pressure and the resulting residue was purified by a flash chromatography(5% AcOEt in hexane). 1H NMR (400 MHz, MeOD) δ 1.20-1.34 (m, 1H), 1.43-1.62 (m, 4H), 1.75-1.85 (m, 1H), 2.61-2.80 (m, 2H), 3.36-3.54 (m, 2H), 3.85-3.95 (m, 1H), 7.12-7.32 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481733B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-d6fd9e33413e407ba1cf82c3c96568b5
출처 메모uspto-grants-2013_07