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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369581Generated: October 28, 2026

Dicyclohexylcarbodiimide → HCID 178463132, compound

https://huagongshe.com/reaction/369581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-methylsulfonyl-3-(3-oxetanyloxy)benzoic acidHCID 23282342—
ReactantHCID 178418331HCID 178418331—
CatalystAcetone CyanohydrinHCID 6406—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 178463132HCID 178463132—

Reaction Steps

Dicyclohexylcarbodiimide (0.72 g (3.5 mmol) was added at ambient temperature with stirring to a solution of 1.07 g (3.5 mmol) of 2-chloro-4-methylsulfonyl-3-(3-oxetanyloxy)benzoic acid and 0.45 g (4 mmol) of 1-ethyl-5-hydroxypyrazole in 25 mL of dry acetonitrile. The mixture was allowed to react for about one hour and then was filtered. The solids collected were extracted with dry acetonitrile. The filtrate and extract were combined and 0.69 g (5.0 mmol) of potassium carbonate and a few drops of acetone cyanohydrin were added with stirring at ambient temperature. The mixture was stirred overnight and was then poured into water. The resulting solution was extracted with ether and then acidified with aqueous hydrochloric acid. The mixture obtained was extracted three times with dichloromethane and the three extracts were combined, washed with water, dried over magnesium sulfate, and concentrated by evaporation under reduced pressure. The yellow solid residue was recrystallized from ethanol to obtain 0.77 g (55 percent of theory) of the title compound as a nearly colorless solid melting at 206-2080° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140271
Source datasetuspto-grants-2000_10
ORD IDord-498d8e3dc611407d9a3a068c47567876
Source noteuspto-grants-2000_10