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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829596Generated: October 29, 2026

Acetic Anhydride → 1-Cyclohexyl-1-methylethyl propionate

https://huagongshe.com/reaction/1829596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPropionic anhydrideHCID 31263—
ReactantCyclohexanemethanol, alpha,alpha-dimethyl-HCID 85531—
Reactant1-(3,3-Dimethylcyclohexyl)ethanoneHCID 91388—
ReactantHCID 22053304HCID 22053304—
ReactantHCID 178418332HCID 178418332—
Product1-Cyclohexyl-1-methylethyl propionateHCID 53950442—

Reaction Steps

The following compounds were prepared analogously to the method described in Example 16, except that the alcohol component used was 2-(3,3-dimethylcyclohexyl)-2-propanol, [which can be prepared from methylmagnesium chloride and 1-(3,3-dimethylcyclohexyl)-ethanone by a Grignard reaction] instead of 2-cyclohexyl-2-propanol. The esterification was carried out with acetic anhydride (Example 18) or propionic anhydride (Example 19). Thus, only the spectroscopic data are indicated at this point:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064102B2
Source datasetuspto-grants-2006_06
ORD IDord-ec0827dca01e40d6ae21a2dce57a9f9e
Source noteuspto-grants-2006_06