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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945243Generated: October 25, 2026

Nonan-5-ol → 5-Nonanone

https://huagongshe.com/reaction/1945243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNonan-5-olHCID 12202—
Reactant2-iodobenzenesulfonic AcidHCID 2778247—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventEthyl AcetateHCID 8857—
Product5-NonanoneHCID 10405—

Reaction Conditions

Temperature70 °C

Reaction Steps

8.5 mg (0.03 mmol) of 2-iodobenzenesulfonic acid prepared by Preparation Example 1, 1.48 g (2.4 mmol) of Oxone (registered trademark) and 433 mg (3 mmol) of 5-nonanol were added to 3.75 ml ethyl acetate, and the mixture was heated at 70° C. while being stirred for ten hours. After heating, the mixture was cooled to room temperature, and the insoluble substance was removed by means of filtering. The obtained filtrate was vacuum-concentrated, and diethyl ether is added in the residue, and then an insoluble material was removed by filtering. The obtained filtrate was vacuum-concentrated, and then 5-nonanone was obtained. 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-28c73ddca10b456cb3298d9e9bc6ada1
Source noteuspto-grants-2013_03