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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252687Generated: October 25, 2026

Carbon Dioxide → p-Menthane-3-carboxylic acid

https://huagongshe.com/reaction/252687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantIodineHCID 807—
Reactant2-MethyltetrahydrofuranHCID 7301—
ReactantP-CymeneHCID 7463—
Reactant1,2-DibromoethaneHCID 7839—
Reactant2-Chloro-4-methyl-1-(1-methylethyl)cyclohexaneHCID 85951—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178461633HCID 178461633—
Productp-Menthane-3-carboxylic acidHCID 97896—

Reaction Conditions

Temperature75 °C

Reaction Steps

Magnesium (15.6 g, 50 mesh), 2-methyl-tetrahydrofuran (103 g), para cymene (50 g), iodine (0.1 g), and ethyl magnesium chloride (4 cc) were added under nitrogen to a 1-liter flask equipped with agitation, addition funnel, off-set adaptor for thermometer, gas addition tube, and condenser. The mixture was stirred for 30 min. at 75° C., and then 1,2,-dibromo ethane (4 cc) was slowly added. p-Menth-3-yl chloride (134 g dissolved in para cymene) was then added at a rate of 33 g/hr (0.21 mole/hr). After approximately ½ of the p-menth-3-yl chloride was added, carbon dioxide was concurrently added by bubbling the carbon dioxide into the mixture at a rate of 7.8 g/hr (0.18 mole/hr), and at a temperature of 80° C. After all of the p-menth-3-yl chloride was added, the temperature was raised to 90° C. to complete carbonation. After carbonation was complete, the resultant mixture was hydrolyzed with aqueous hydrochloric acid having a concentration of 15%. VPC analysis showed a yield of 78.3% by weight of p-menthane-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868200B2
Source datasetuspto-grants-2011_01
ORD IDord-f1abae5062114e6182b6e3fad8c6a1a4
Source noteuspto-grants-2011_01