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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849614Generated: November 1, 2026

Methyl iodide → methyl (RS)-2-methyl-5-oxo-2-phenylcyclohexene-1-carboxylate

https://huagongshe.com/reaction/849614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(RS)-2-methyl-5-oxo-2-phenylcyclohexene-1-carboxylic acidHCID 20647081—
SolventAcetoneHCID 180—
Productmethyl (RS)-2-methyl-5-oxo-2-phenylcyclohexene-1-carboxylateHCID 2064708394.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06013662
Source datasetuspto-grants-2000_01
ORD IDord-0e22cebf3e734468bab1519fd7930cdd
Source noteuspto-grants-2000_01