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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610693Generated: October 31, 2026

Carbon Dioxide → Benzoic acid, 3-(1-methylethyl)-

https://huagongshe.com/reaction/1610693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant1,2-DibromoethaneHCID 7839—
Reactant1-Bromo-3-isopropylbenzeneHCID 138499—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductBenzoic acid, 3-(1-methylethyl)-HCID 138552—

Reaction Conditions

Temperature70 °C

Reaction Steps

While stirring a solution of powdery magnesium (3.33 g, 137 mmol) and iodine (one crumb) in tetrahydrofuran (10 ml), a solution of 3-isopropylbromobenzene (10.91 g, 54.80 mmol) and 1,2-dibromoethane (10.3 g, 54.8 mmol) in tetrahydrofuran (100 ml) was dropwise added slowly. After completion of the dropwise addition, the mixture was stirred at 70° C. for 1 hr. The reaction solution was cooled to −78° C., and pulverized dry ice (10 g) was carefully added. 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 to give a crude product of 3-isopropylbenzoic acid as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-65efc7f73ba9418aa715cdae44e12f8e
Source noteuspto-grants-2006_01