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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076795Generated: November 1, 2026

Acetic Acid → HCID 527056, compound

https://huagongshe.com/reaction/1076795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-2-butenoneHCID 62002—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 527056HCID 527056—

Reaction Steps

10 ml of acetic anhydride were first added to a solution kept at 10° of 3.5 g of Na2Cr2O7 .2H2O in 10 ml of acetic acid and the obtained mixture was stirred for one hour. A solution of 2.1 g of 2,6,6-trimethyl-1-(but-2-enoyl)-cyclohex-2-ene [prepared according to the method described in Helv. Chim. Acta 53, 541 (1970)], in 10 ml of acetic anhydride was then added to the above mixture. After having been stirred overnight at room temperature, the reaction mixture was then poured onto crushed ice and extracted with ether. After the usual treatments of washing, drying and evaporation, there was obtained 2.0 g of crude material containing 80 % of the desired keto compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03957877
Source datasetuspto-grants-1976_05
ORD IDord-44fc53604a894482b08acc8e8afef30f
Source noteuspto-grants-1976_05