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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328059Generated: October 29, 2026

Nitromethane → 2-n-Hexyl-3-nitromethylcyclopentanone

https://huagongshe.com/reaction/328059

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 numberUS04016109
Source datasetuspto-grants-1977_04
ORD IDord-efbadcba02dd41b886da66b6e6c9c1d4
Source noteuspto-grants-1977_04