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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416946Generated: November 2, 2026

1-Nonanol, 9-bromo- → 9-Bromononanoic Acid

https://huagongshe.com/reaction/2416946

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Nonanol, 9-bromo-HCID 108700—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
Product9-Bromononanoic AcidHCID 54822177%

Reaction Steps

2 N Jones' reagent (20 ml) was gradually and dropwise added to an acetone (20 ml) solution of 9-bromononanol (2.2 g,10 mmols) with cooling with ice, and then stirred at room temperature for 10 minutes. The reaction mixture was extracted three times with hexane (40 ml). The organic layer was washed with water, and then extracted three times with an aqueous saturated solution of potassium carbonate (40 ml). The aqueous layers were combined, then made acidic (pH=1) with 10% sulfuric acid added thereto, and extracted with ethyl acetate. The resulting organic layer was washed with water and saturated saline in that order, and dried with anhydrous sodium sulfate, and the solvent was evaporated. 1.8 g (yield: 77%) of 9-bromononanoic acid was obtained as colorless needle-like crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825223B2
Source datasetuspto-grants-2004_11
ORD IDord-65cc00d5c6bd46f3aa80c7a35716e29d
Source noteuspto-grants-2004_11