HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → N,N'-Dicyclohexylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | (Boc-aminooxy)acetic acid | HCID 2755974 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N,N'-Dicyclohexylurea | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07316999B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-aa3c5d6c3ee7456b988e1514de59ee6f |
| Source note | uspto-grants-2008_01 |