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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033470Generated: October 27, 2026

Hydrochloric Acid → 2,8-Dimethyl-5-nonanol

https://huagongshe.com/reaction/1033470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl formateHCID 8025—
ReactantPotassium HydroxideHCID 14797—
ReactantDiisoamyl ketoneHCID 62421—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant2,8-Dimethyl-5-nonanolHCID 557851—
ReactantHCID 178418529HCID 178418529—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2,8-Dimethyl-5-nonanolHCID 557851—
Product2,8-Dimethylnonan-5-one oximeHCID 15029999—

Reaction Steps

To a solution of 5.11 g of 2,8-dimethylnonan-5-one (b.p.: 103°-105° C./19 mmHg, prepared by oxidizing 2,8-dimethylnonan-5-ol with a bleaching powder; 2,8-dimethylnonan-5-ol was prepared by reaction of ethyl formate and isoamylmagnesium bromide) in 20 ml of ethanol were successively added an aqueous solution of 3.47 of hydroxylamine hydrochloride in 6 ml of water and a solution of 4.77 g of potassium hydroxide in 6 ml of water. The mixture was heated under reflux. The reaction mixture was then poured into 150 ml of ice-containing water. The aqueous mixture was made acidic by addition of 2N hydrochloric acid and extracted with benzene. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and evaporated under reduced pressure to remove the solvent. There was obtained 5.21 g of 2,8-dimethylnonan-5-one oxime as a pale brown oil, yield: 93.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310902
Source datasetuspto-grants-1994_05
ORD IDord-cd85ebe6c9c94127b6a30e6e0ae6a368
Source noteuspto-grants-1994_05