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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945259Generated: October 31, 2026

Nonan-5-ol → 5-Nonanone

https://huagongshe.com/reaction/1945259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNonan-5-olHCID 12202—
Reactant2-Iodo-5-methylbenzoic acidHCID 142941—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventNitromethaneHCID 6375—
Product5-NonanoneHCID 10405—

Reaction Conditions

Temperature70 °C

Reaction Steps

1.57 mg (0.006 mmol) of 2-iodo-5-methylbenzoic acid prepared by Preparation Example 3, 1.11 g (1.8 mmol) of powdered Oxone (registered trademark) and 433 mg (3 mmol) of 5-nonanol were added to 3.75 ml of nitromethane, and the mixture was heated at 70° C. while being stirred for 12 hours. After being heated, the mixture was cooled to room temperature, and the insoluble substance was removed by means of filtering. Water was added in the filtrate, extraction was carried out using diethyl ether. The organic phase was dried by using sodium sulfate, and then 5-nonanone was obtained by means of vacuum-concentration. The yield of the obtained 5-nonanone was determined and the result is shown in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394995B2
Source datasetuspto-grants-2013_03
ORD IDord-28d804917361414e816455430fceb2de
Source noteuspto-grants-2013_03