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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917622Generated: October 31, 2026

Carbon Dioxide → 2,4,6-Trichloropyrimidine-5-carboxylic acid

https://huagongshe.com/reaction/917622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
Reactant2,4,6-TrichloropyrimidineHCID 77378—
ReactantButyllithiumHCID 178418339—
SolventSodium ChlorideHCID 5234—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2,4,6-Trichloropyrimidine-5-carboxylic acidHCID 20083957—

Reaction Steps

A mixture of diisopropylamine 2.54 g, a 1.6M solution of n-butyl lithium in hexane 15.7 ml and tetrahydrofuran 100 ml is stirred for 30 minutes on a dry ice-acetone bath. Thereto is added 2,4,6-trichloropyrimidine 2.00 g in tetrahydrofuran 8 ml over a period of 30 minutes, followed by further one hour agitation. The reaction mixture is poured into dry ice, and the mixture is stirred for a hour at room temperature. The reaction mixture is made acidic with 10% hydrochloric acid 20 ml, diluted with an aqueous saturated sodium chloride solution and extracted with ethyl acetate. The organic layer is washed, dried and concentrated in vacuo. The solvent is removed by azeotrope with chloroform and the resulting hemisolid is triturated with hexane to give 5-carboxy-2,4,6-trichloropyrimidine as a crystalline powder, 1.51 g. mp 150-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273868B2
Source datasetuspto-grants-2007_09
ORD IDord-7085751fddfa434fa6dc2f92cb5bddde
Source noteuspto-grants-2007_09