HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328059Generated: October 29, 2026
Nitromethane → 2-n-Hexyl-3-nitromethylcyclopentanone
https://huagongshe.com/reaction/328059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 2-Hexyl-2-cyclopenten-1-one | HCID 66768 | — |
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-n-Hexyl-3-nitromethylcyclopentanone | HCID 21443737 | — |
Reaction Steps
In a 2-L flask fitted with a reflux condenser, is placed 332 g of 2-n-hexyl-2-cyclopentenone, 183 g of nitromethane, 30 ml of 40% methanolic solution of benzyltrimethylammonium hydroxide (Triton B) and 200 ml of dry dioxane. The reaction mixture is refluxed for 23 hours. The solvent is distilled off under a reduced pressure and the residue is dissolved in 1 L of ether. The ether solution is washed successively with dilute hydrochloric acid, water and sodium bicarbonate solution and dried over anhydrous sodium sulphate. The solvent is removed at atmospheric pressure and the residue is distilled through a short Vigreux column. After a lower boiling fraction (35 g, 65° C/0.2 mm) consisting of 2-n-hexyl-2-cyclopentenone, the product is collected at 135° C/0.3 mm, yield 365 g (80%), nD20 1.4733.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04016109 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-efbadcba02dd41b886da66b6e6c9c1d4 |
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| Source note | uspto-grants-1977_04 |
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