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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683303Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 178473054, compound

https://huagongshe.com/reaction/1683303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBis(1,1-dimethylethyl) [[(8-aminooctyl)imino]methylene]biscarbamateHCID 25214054—
ReactantEthyl 2-phenylmethoxypropanedioateHCID 86750947—
SolventDichloromethaneHCID 6344—
ProductHCID 178473054HCID 17847305440.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

2.6 g (10.9.10-3 mol) of ethyl 2-phenylmethoxypropanedioate are dissolved in 50 ml of dichloromethane and the mixture is cooled to 0° C. 4.34 g (22.10-3 mol) of N,N'-dicyclohexylcarbodiimide and 0.57 g (4.10-3 mol) of 1-hydroxybenzotriazole are added, the mixture is stirred for 0.5 hour, a solution of 4.21 g (10.9. 10-3 mol) of bis(1,1-dimethylethyl) [[(8-aminooctyl)imino]methylene]biscarbamate in 15 ml of dichloromethane is then added and the mixture is stirred at room temperature for 48 hours. The reaction medium is concentrated under reduced pressure and the residue is then purified by chromatography on silica using a methylcyclohexane/ethyl acetate mixture (7/3) as the eluent to give 2.7 g (yield=40.8%) of the expected product in the form of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637613
Source datasetuspto-grants-1997_06
ORD IDord-2ef0cf1e539e45c69803c5fb9e2aecdb
Source noteuspto-grants-1997_06