HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5980Generated: October 25, 2026
Pentane → ethyl 5-[(E)-(2-imidazol-1-yl-3,4-dihydro-2H-naphthalen-1-ylidene)amino]oxypentanoate
https://huagongshe.com/reaction/5980
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pentane | HCID 8003 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 5-bromovalerate | HCID 84580 | — |
| Reactant | (NE)-N-(2-imidazol-1-yl-3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamine | HCID 88465041 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 5-[(E)-(2-imidazol-1-yl-3,4-dihydro-2H-naphthalen-1-ylidene)amino]oxypentanoate | HCID 19794644 | — |
Reaction Steps
(+-)-(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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05246956 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-461d76bc7b794e33b5c526fa6f430a5a |
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| Source note | uspto-grants-1993_09 |
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