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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29168생성일: 2026년 10월 23일

Cyclohexyl bromide → N-cyclohexyloxyphthalimide

https://huagongshe.com/ko/reaction/29168

반응식

참여 물질

역할이름HCID투입량
반응물Cyclohexyl bromideHCID 7960—
반응물N-HydroxyphthalimideHCID 10665—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
용매DimethylformamideHCID 6228—
생성물N-cyclohexyloxyphthalimideHCID 10467039—

반응 조건

온도55 °C

반응 단계

N-hydroxylphthalimide (61.3 mmol, 10.0 g) was dissolved in anhydrous DMF (60 mL) under nitrogen. To the stirring solution, DBU (92.0 mmol, 13.75 mL) was injected followed by cyclohexyl bromide (76.6 mmol, 9.43 mL) and the reaction was warmed to 55° C. After stirring for 15 hours, the reaction was warmed to 80° C. for 5 hours, then cooled to room temperature and concentrated to a red oil. The reaction was partitioned between ethyl acetate and 1N HCl. The organic layer was washed with 1N NaOH, brine and dried over magnesium sulfate. The solvent was removed under vacuum and the crude product was triturated with hexanes providing 2.89 g (19%) of a yellow solid. Rf: 0.7 (2:1 hexanes/ethyl acetate); H1-NMR (CDCl3): δ 7.80 (2H,m), 7.73(2H,m), 4.21 (1H,m), 2.02-1.98 (2H,m), 1.87-1.82 (2H,m), 1.59-1.53 (4H,m), 1.30-1.24 (2H,m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419967B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-16dd12d525704f8bb2157302ec748a15
출처 메모uspto-grants-2008_09