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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376251Generated: October 27, 2026

Lithium diisopropylamide → Ethyl 2-(2-chloro-6-fluorophenyl)-3-(4-methylcyclohexyl)-3-oxopropionate

https://huagongshe.com/reaction/376251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl 2-chloro-6-fluorophenylacetateHCID 2733231—
Reactant4-Methylcyclohexane-1-carbonyl chlorideHCID 12986357—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(2-chloro-6-fluorophenyl)-3-(4-methylcyclohexyl)-3-oxopropionateHCID 19361668106.5%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Lithium diisopropylamide (0.18 mol) in tetrahydrofuran (270 ml) is added to a mixture of ethyl (2-chloro-6-fluorophenyl)acetate (38.1 g, 0.175 mol) and THF (200 ml) at -70° C. The reaction mixture is stirred for 2 hours at about -70° C. 4-Methylcyclohexanecarboxylic acid chloride (28.25 g, 0.175 mol) is added and the reaction mixture is allowed to warm up to room temperature over night. The reaction mixture is then quenched with hydrochloric acid (5N, 60 ml) and most of the organic solvent is distilled off under reduced pressure. From the remainder the product is extracted with light petroleum (200 ml). The organic layer is separated, washed with water, dried with magnesium sulphate and concentrated in vacuo to yield a yellow oil (63.5 g). This is filtered through silica (light petroleum, 3% ethyl acetate) to yield a pale yellow oil (27.2 g). The product is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020338
Source datasetuspto-grants-2000_02
ORD IDord-11271ffa8afd4c7da6c27ef32e409b42
Source noteuspto-grants-2000_02