HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554229Generated: October 28, 2026
Cyclohexyl bromide → HCID 66925034, compound
https://huagongshe.com/reaction/554229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexyl bromide | HCID 7960 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Ethyl 1H-pyrrole-3-carboxylate | HCID 13070719 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | HCID 66925034 | HCID 66925034 | 16% |
Reaction Steps
Under an argon atmosphere, to a solution of ethyl 1H-pyrrole-3-carboxylate (2.09 g) and aluminum(III) chloride (4.0 g) in carbon disulfide (30 mL) was added bromocyclohexane (1.84 mL) under ice-cooling with stirring, and the mixture was stirred at room temperature for 30 min. The mixture was heated to 50° C., and stirred for 2 hr. The reaction product was cooled to room temperature, poured into ice water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1→8:2), and recrystallized from hexane to give the title compound as a colorless solid (yield 530 mg, 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048909B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-62cee19ab8e14936ba829df650d901c8 |
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| Source note | uspto-grants-2011_11 |
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