HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → methyl (RS)-2-methyl-5-oxo-2-phenylcyclohexene-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | (RS)-2-methyl-5-oxo-2-phenylcyclohexene-1-carboxylic acid | HCID 20647081 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | methyl (RS)-2-methyl-5-oxo-2-phenylcyclohexene-1-carboxylate | HCID 20647083 | 94.2% |
Reaction Steps
0.88 cm3 (14 mmol) of methyl iodide and 1.8 cm3 (12 mmol) of 1,8-diazabicyclo[5.4.0]undec-7-ene, dropwise, were successively added to a solution of 2.3 g (10 mmol) of (RS)-2-methyl-5-oxo-2-phenylcyclohexene-1-carboxylic acid in 20 cm3 of acetone. The reaction mixture was subsequently heated at reflux for two hours. The acetone was subsequently concentrated, the residue was then stirred with 100 cm3 of water and then extracted with three times 30 cm3 of ethyl acetate. After drying over magnesium sulphate and concentrating under reduced pressure, 2.3 g (94%) of methyl (RS)-2-methyl-5-oxo-2-phenylcyclohexene-1-carboxylate were obtained in the form of an orange oil, the characteristic of which was as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124465 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-850d69f68f624b36ba44957a1d85b68a |
| Source note | uspto-grants-2000_09 |