HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368758Generated: October 31, 2026
1,5-Dibromopentane → (5-Bromopentyl)cyclohexane
https://huagongshe.com/reaction/2368758
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178419651 | HCID 178419651 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (5-Bromopentyl)cyclohexane | HCID 14952366 | — |
Reaction Steps
A mixture of 1,5-dibromopentane (16 gm, 69.97 mmol) in THF (20 ml) and a solution of (Li2CuCl4 in ether, 14 ml) under nitrogen at 5-10° C. was stirred for 25 minutes and then cyclohexyl magnesium bromide (10 gm, 69.97 mmol) was added dropwise over 30 minutes. The reaction was stirred at 0° C. for another 1 h, then at room temperature for 12 hr. The reaction mixture was cooled to 0° C., saturated with NH4Cl solution (20 ml), diluted with ethyl acetate (100 ml) and the combined organic layer was separated, washed with brine and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the crude product was purified by column chromatography using hexane as an eluent. The pure product was an oily liquid (12.84 gm). 1H NMR (CDCl3): 0.8 (t, 2H, J=10.2 Hz), 1.00-1.38 (m, 9H), 1.52-168 (m, 6H), 1.70-1.80 (m, 2H), 3.38 (t, 2H, J=7.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703798B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-cf3953efd78d4e9696fe43325bc070cb |
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| Source note | uspto-grants-2014_04 |
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