Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654026Generated: October 29, 2026

Dicyclohexylcarbodiimide → HCID 15057637, compound

https://huagongshe.com/reaction/654026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactantalpha-(Aminomethyl)-2,2-dimethyl-1,3-dioxolane-4-methanolHCID 11971028—
ReactantHCID 15057636HCID 15057636—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
ProductHCID 15057637HCID 15057637—

Reaction Conditions

Temperature-10 °C

Reaction Steps

5.96 g (18 mmol) of 3-[N-(2,4,6-trifluorophenyl)sulfamoyl]-benzoic acid is dissolved in 50 ml of dry dimethylformamide under argon atmosphere, 2.76 g (18 mmol) of hydroxybenzotriazole and 2.9 (18 mmol) of 2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamine are added and the solution is cooled to -10° C. At this temperature, 3.71 g (18 mmol) of dicyclohexylcarbodiimide is added to the solution. Then it is stirred for 1 hour at -10° C. and 6 hours at room temperature. The turbid reaction solution is filtered and the filtrate is concentrated by evaporation in a vacuum. The residue is dissolved in 100 ml of ethyl acetate, the solution is shaken out five times with saturated sodium bicarbonate solution and twice with water, the organic phase is dried on sodium sulfate, filtered and concentrated by evaporation. The residue is chromatographed on silica gel 60 (Merck) with ethyl acetate/hexane. 4.91 g (10.35 mmol)=57.5% of the theoretical yield is obtained as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05130119
Source datasetuspto-grants-1992_07
ORD IDord-862f74937cb94db983076561833e83ff
Source noteuspto-grants-1992_07