HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920128Generated: October 30, 2026
1,5-Dibromopentane → HCID 178453979, compound
https://huagongshe.com/reaction/1920128
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178419079 | HCID 178419079 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178453979 | HCID 178453979 | 37.4% |
Reaction Steps
Trans-4-tert-butoxycarbonylamino-aminocyclohexane (1 g) and potassium carbonate (1.3 g) were suspended in ethanol (20 mL), and then 1,5-dibromopentane (1.07 g) was added thereto. The reaction solution was stirred at 80° C. for 48 hours. After the reaction solution was cooled to room temperature, the solvent was concentrated under reduced pressure. The residue was dissolved in water (50 mL). The aqueous layer was extracted twice with dichloromethane (50 mL). The combined organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate. After removing the anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by silica gel chromatography (ethyl acetate: 10%-saturated aqueous ammonia-methanol=1:0→10:1) to obtain the title compound (492 mg) having the following physical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08168783B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-6e9b8862df2945e48b7be9b0604850c7 |
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| Source note | uspto-grants-2012_05 |
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