Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973202Generated: October 30, 2026

2-Butanone, 4-(2,6,6-trimethyl-1,3-cyclohexadien-1-yl)- → HCID 19857690, compound

https://huagongshe.com/reaction/1973202

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butanone, 4-(2,6,6-trimethyl-1,3-cyclohexadien-1-yl)-HCID 577126—
Reactant36208-32-9HCID 6431122—
ProductHCID 19857690HCID 19857690—

Reaction Steps

4-(2,6,6-TRIMETHYL-1,3-CYCLOHEXADIEN-1-YL)-2-BUTANONE HAVING THE STRUCTURE: ##STR2## may be synthesized according to the technique of Wolf and Zink, Volume 56, Helvetica Chimica Acta., Fasc 3 (1973) pp. 1062-1066, or according to Examples I and II of Rowland, U.S. Pat. No. 3,436,421 issued on Apr. 1, 1969 by means of bromination of -dihydroionone followed by debromination. 4-(6,6-dimethyl-2-methylene-3-cyclohexen-1-yl)-2-butanone having the structure: ##STR3## is also produced in this process as a bi-product thereof (B.P. 65° C at 0.15 mm Hg. pressure). 4-(2,6,6-trimethyl-1,3-cyclohexadien-1-yl)-2-butanone is also shown to be a bi-product in the cyclization of ionone to beta ionone by Kruk and De Boer in Volume 87 Recueil (1968) pp. 641-654 as an intermediate in preparing other perfumery compounds. The compound having the structure: ##STR4## is disclosed in Japanese Patent No. 7121,015 (Sakan and Isoe)issued June 14, 1971.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03996296
Source datasetuspto-grants-1976_12
ORD IDord-fd26229e140749c8ba22cb1165badd3e
Source noteuspto-grants-1976_12