Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180472Generated: November 1, 2026

Dicyclohexylcarbodiimide → HCID 131726110, compound

https://huagongshe.com/reaction/1180472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-Bromopropionic acidHCID 11729—
ReactantEther hydrochlorideHCID 10953452—
ReactantHCID 131726111HCID 131726111—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 131726110HCID 131726110—

Reaction Steps

Bromopropionic acid anhydride [formed by reacting bromopropionic acid (1.66 g, 10.86 mmol) with DCC (1.12 g, 5.43 mmol) in 20 ml anhydrous dichloromethane for 15 minutes at 25° C., and filtering off the solid that precipitated] was added to a solution of aminophenylarsineoxide (1 g, 5.43 mmol, synthesized according to published protocol) in 10 ml DMF, and allowed to stir overnight. The amino phenylarsineoxide was rendered soluble by adding to it 10.86 mmol HCl/ether followed by neutralization with triethylamine and filtering away the solid that formed. The solution was quenched with 20 ml water, and filtered to remove solids. The filtrate was evaporated to an oil, and purified via FlAsH chromatography. In later preparations, 3-bromopropionyl chloride was used instead of the anhydride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282373B2
Source datasetuspto-grants-2007_10
ORD IDord-68aed339872d46eea12091caa1e964ab
Source noteuspto-grants-2007_10