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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250311Generated: October 31, 2026

Ethyl Acetate → N,N'-Dicyclohexylurea

https://huagongshe.com/reaction/2250311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant(Boc-aminooxy)acetic acidHCID 2755974—
SolventAcetonitrileHCID 6342—
ProductN,N'-DicyclohexylureaHCID 4277—

Reaction Steps

tert-Butyloxycarbonylaminoxy acetic acid was dissolved in ice-cooled ethyl acetate or acetonitrile and treated with N,N′-dicyclohexylcarbodiimide (1.0 equivalent) and N-hydroxysuccinimide (1.0 equivalent). The reaction mixture was stirred at room temperature overnight. The N,N′-dicyclohexylurea formed was removed by filtration and the filtrate was evaporated to dryness in vacuo. The crude Boc-AOA-OSu was either used directly in the next step or purified by recrystallisation from chloroform. Adopted from Kurth et al. J. Med. Chem. 1993, 36, 1255.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07316999B2
Source datasetuspto-grants-2008_01
ORD IDord-aa3c5d6c3ee7456b988e1514de59ee6f
Source noteuspto-grants-2008_01