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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076041Generated: November 1, 2026

Nitromethane → 2-n-Hexyl-3-nitromethylcyclopentanone

https://huagongshe.com/reaction/1076041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
Reactant2-Hexyl-2-cyclopenten-1-oneHCID 66768—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Solvent1,4-DioxaneHCID 31275—
Product2-n-Hexyl-3-nitromethylcyclopentanoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954834
Source datasetuspto-grants-1976_05
ORD IDord-36392b488c844ca38e6863594c57be6d
Source noteuspto-grants-1976_05