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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236228Generated: October 25, 2026

Hydrochloric Acid → HCID 178481844, compound

https://huagongshe.com/reaction/236228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-(methylsulfonyl)benzoic acidHCID 735863—
ReactantHCID 178481816HCID 178481816—
SolventChloroformHCID 6212—
Solventtert-ButanolHCID 6386—
ProductHCID 178481844HCID 17848184453%

Reaction Steps

2-chloro-4-methanesulfonyl benzoic acid 3.87 g (0.0165 mol) was added to 40 ml of tert.-butanol, and then were added thereto 3.47 g (0.0168 mol) of N,N'-dicyclohexylcarbodiimide and 1.21 g (0.088 mol) of anhydrous potassium carbonate. The resulting mixture was incorporated with 1.65 g (0.0168 mol) of 1-methyl-5-hydroxypyrazole with stirring at room temperature and heated at 60° C. to effect reaction for 5 hours. After completion of the reaction, solvent was distilled away from the reaction mixture under reduced pressure and the resulting residue was washed with chloroform. Thereafter, the residue was incorporated with 30 ml of water and stirred. Insoluble matter was filtered out. The aqueous solution thus obtained was incorporated with conc. hydrochloric acid to adjust the pH thereof to 1 or lower and then with chloroform to effect extraction. An organic layer was separated, dried over anhydrous sodium sulfate, freed of solvent by distillation under reduced pressure, and dried to give 2.75 g of the final product (yield: 53%), m.p. 272°-275° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04643757
Source datasetuspto-grants-1987_02
ORD IDord-9de8fd284a304d859132ddddaa3258ef
Source noteuspto-grants-1987_02