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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5980생성일: 2026년 10월 23일

Pentane → ethyl 5-[(E)-(2-imidazol-1-yl-3,4-dihydro-2H-naphthalen-1-ylidene)amino]oxypentanoate

https://huagongshe.com/ko/reaction/5980

반응식

참여 물질

역할이름HCID투입량
반응물PentaneHCID 8003—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 5-bromovalerateHCID 84580—
반응물(NE)-N-(2-imidazol-1-yl-3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamineHCID 88465041—
용매DimethylformamideHCID 6228—
생성물ethyl 5-[(E)-(2-imidazol-1-yl-3,4-dihydro-2H-naphthalen-1-ylidene)amino]oxypentanoateHCID 19794644—

반응 단계

(+-)-(E)-2-(1H-imidazol-1-yl)-1,2,3,4-tetrahydronaphtalen-1-one oxime (500 mg; 2.2 mmoles) dissolved in dry DMF (27 ml) is added, under dry nitrogen atmosphere, to a pentane-washed sodium hydride suspension (160 mg NaH 55%; 3.6 mmoles), in dry DMF (10 ml). The resulting reaction mixture is stirred at r.t. for 2 hours. Then ethyl-5-bromopentanoate (0.530 ml; 3.3 mmoles) is added at r.t. and the reaction mixture is stirred at r.t. for 3 hrs., the solvent evaporated in vacuo, and the residue carefully taken up with ice-cooled water and extracted with ethyl acetate. The collected organic phases are dried over Na2SO4 and evaporated to give an oily crude material which is chromatographed over silica gel. By eluting with CH2Cl2 /MeOH (95:5), the pure title compound is obtained as a slight yellow oil (250 mg). 1H-NMR (200MH2, CDCl3) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246956
출처 데이터셋uspto-grants-1993_09
ORD IDord-461d76bc7b794e33b5c526fa6f430a5a
출처 메모uspto-grants-1993_09