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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1269749생성일: 2026년 10월 25일

tert-Butanol → 1-Benzyl-3-(tritylamino)-2-azepanone

https://huagongshe.com/reaction/1269749

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물3-(Tritylamino)-2-azepanoneHCID 14729218—
촉매Tetrabutylammonium IodideHCID 67553—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-3-(tritylamino)-2-azepanoneHCID 6943101463%

반응 단계

To a suspension of 3-(tritylamino)-2-azepanone (2.85 g, 7.69 mmol) in tetrahydrofuran (30 ml) was added 60%-sodium hydride (462 mg, 11.6 mmol) at 0° C., and then stirred at room temperature for 30 minutes. Subsequently, a solution of benzyl bromide (1.0 ml, 8.41 mmol) in tetrahydrofuran (5 ml) was added dropwise thereto at room temperature over a period of 3 minutes, followed by adding thereto tetra-n-butylammonium iodide (57 mg, 0.15 mmol), and the resulting mixture was stirred at room temperature for 6 hours. The reaction mixture was cooled on an ice-water bath and t-butanol (0.7 ml) and water (1 ml) were added thereto at 0° C. The resulting mixture was poured into water and then extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: n-hexane/chloroform) to obtain 1-benzyl-3-(tritylamino)-2-azepanone (2.22 g, 63%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07199147B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-e20b0a807e764389869a1afb2e11ee16
출처 메모uspto-grants-2007_04