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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260935Generated: October 31, 2026

1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-one → HCID 68635470, compound

https://huagongshe.com/reaction/2260935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-oneHCID 42296—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl cysteinate hydrochlorideHCID 2723617—
SolventEthanolHCID 702—
ProductHCID 68635470HCID 6863547071%

Reaction Steps

A solution of 1-(2,6,6-trimethylcyclohex-3-enyl)but-2-en-1-one (83.0 g, 0.50 mol, 2 equiv.), ethyl diisopropylamine (32.3 g, 0.25 mol, 1 equiv.) and L-Cystein ethyl ester hydrochloride (46.5 g, 0.25 mol, 1 equiv.) in EtOH (600 ml) is heated to 60° C. during 44 h. The solvent is removed in vacuo and the residue dissolved in methyl t-butyl ether. The solution is washed with dilute aq. NaCl, dried over MgSO4 and concentrated. The residue is purified by chromatography on SiO2 to yield 85.5 g (71%) of the title compound as orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846887B2
Source datasetuspto-grants-2010_12
ORD IDord-dc337b6f740e46d58b97be5ced8deaf8
Source noteuspto-grants-2010_12