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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610671Generated: October 31, 2026

Carbon Dioxide → beta-Phenylisovaleric acid

https://huagongshe.com/reaction/1610671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant1,2-DibromoethaneHCID 7839—
ReactantNeophyl chlorideHCID 68191—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Productbeta-Phenylisovaleric acidHCID 13890—

Reaction Conditions

Temperature60 °C

Reaction Steps

While stirring powdery magnesium (9.56 g, 393 mmol) and iodine (one crumb) in tetrahydrofuran (10 ml), a solution of 1-chloro-2-methyl-2-phenylpropane (26.53 g, 157.3 mmol) and 1,2-dibromoethane (29.6 g, 157 mmol) in tetrahydrofuran (100 ml) was dropwise added at a rate permitting the reaction solution to gently reflux. After completion of the dropwise addition, the mixture was stirred at 60° C. for 4 hrs. The reaction solution was cooled to −78° C., and pulverized dry ice (50 g) was carefully added. After completion of the dropwise addition, the reaction solution was gradually warmed to room temperature with stirring. The reaction solution was diluted with water, acidified with conc. hydrochloric acid, and extracted twice with ethyl acetate. The solvent of the recovered organic layer was evaporated under reduced pressure. The obtained residue was mixed with sodium hydroxide (6 g) and water (200 ml). The obtained aqueous solution was washed with diethyl ether-hexane, acidified with conc. hydrochloric acid, and extracted twice with ethyl acetate. The recovered organic layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure to give the objective substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-88473e8ee69742858af0bd2a40390dd5
Source noteuspto-grants-2006_01