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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255163Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 86747153, compound

https://huagongshe.com/reaction/2255163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantPropanedioic acid, 2-amino-, 1,3-diethyl esterHCID 81272—
Reactant(+-)-2-Hydroxyisocaproic acidHCID 92779—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86747153HCID 86747153—

Reaction Steps

30 Milliliters of water and 7.0 g of sodium hydrogen carbonate were added to a suspension of 17.5 g of diethyl aminomalonate hydrochloride in 150 ml of dichloromethane. After 20 minutes, the dichloromethane layer was separated and dried over magnesium sulfate. The solvent was removed by evaporation under reduced pressure to obtain colorless oily diethyl aminomalonate. The diethyl aminomalonate was made into a solution of the diethyl aminomalonate, 10.0 g of α-hydroxyisocaproic acid and 8.7 g of N-hydroxysuccinimide dissolved in 200 ml of dioxane. To the solution was added 15.7 g of N,N'-dicyclohexylcarbodiimide. The mixture was stirred for 16 hours at room temperature and then filtered. The filtrate was subjected to removal of the solvent by evaporation. The residue was mixed with ethyl acetate, and the mixture was washed with 10% hydrochloric acid, water, an aqueous solution saturated with sodium hydrogen carbonate, and an aqueous solution saturated with NaCl solution in this order, and dried over magnesium sulfate. The solvent was removed by evaporation to obtain 29.19 g of diethyl N-(2-hydroxyimino- 4-methylpentanoyl)aminomalonate (Compound B-25) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05238938
Source datasetuspto-grants-1993_08
ORD IDord-ef31f401088a47ffb34818fdf6261a76
Source noteuspto-grants-1993_08