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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649968Generated: October 31, 2026

Acetic Anhydride → HCID 54267635, compound

https://huagongshe.com/reaction/1649968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 10888318HCID 10888318—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 54267635HCID 54267635—

Reaction Steps

The general method for the preparation of the starting enol esters is illustrated by the following example: 0.063M of 3,3,7-trimethyl-oct-6-ene-1-al were added under stirring to a mixture consisting of 0.06M of triethylamine, 0.126M of acetic anhydride and 1.1 g of potassium acetate pre-heated to 80°. The reactive mixture was refluxed for approximately 7 h. After cooling to room temperature, toluene and water were added and the two phases separated. 3,3,7-Trimethyl-1,6-octadienyl acetate was then obtained as a toluene solution and finally isolated by evaporation at reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04922027
Source datasetuspto-grants-1990_05
ORD IDord-d169eb32a8744f0b9eaf3e8218e59bdb
Source noteuspto-grants-1990_05