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HRID 5980作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物PentaneHCID 8003—
反応物Sodium hydrideHCID 24758—
反応物Ethyl 5-bromovalerateHCID 84580—
反応物(NE)-N-(2-imidazol-1-yl-3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamineHCID 88465041—
溶媒DimethylformamideHCID 6228—
生成物ethyl 5-[(E)-(2-imidazol-1-yl-3,4-dihydro-2H-naphthalen-1-ylidene)amino]oxypentanoateHCID 19794644—

反応手順

(+-)-(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246956
出典データセットuspto-grants-1993_09
ORD IDord-461d76bc7b794e33b5c526fa6f430a5a
出典メモuspto-grants-1993_09