HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-one → HCID 68635470, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-one | HCID 42296 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl cysteinate hydrochloride | HCID 2723617 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68635470 | HCID 68635470 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846887B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-dc337b6f740e46d58b97be5ced8deaf8 |
| Source note | uspto-grants-2010_12 |