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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726527Generated: October 31, 2026

Acetic Anhydride → 4-Acetoxy-3-nitrohexane

https://huagongshe.com/reaction/1726527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Nitro-3-hexanolHCID 220638—
CatalystSulfuric AcidHCID 1118—
SolventChloroformHCID 6212—
Product4-Acetoxy-3-nitrohexaneHCID 1176930286.1%

Reaction Steps

4-hydroxy-3-nitrohexane (14.7 g, 100 mmol), acetic anhydride (14.8 ml, 157.3 mmol), chloroform (50 ml), and several drops of concentrated sulfuric acid were fed into a reaction vessel, and the mixture was stirred at room temperature for 10 hours. After the completion of the reaction, chloroform (50 ml) was added, and the whole was washed with water, a 5% aqueous solution of baking soda, and a saturated salt solution. The organic layer was dried with anhydrous sodium sulfate and concentrated under reduced pressure to yield 4-acetoxy-3-nitrohexane (16.3 g, 86% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491967B2
Source datasetuspto-grants-2009_02
ORD IDord-927bc4fdaf7345fbb0b9c776f08ebcca
Source noteuspto-grants-2009_02