HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N'-Dicyclohexylurea → 1-[(3-Hydroxybenzoyl)oxy]pyrrolidine-2,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N'-Dicyclohexylurea | HCID 4277 | — |
| Reactant | 3-Hydroxybenzoic Acid | HCID 7420 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[(3-Hydroxybenzoyl)oxy]pyrrolidine-2,5-dione | HCID 20310802 | — |
Reaction Steps
As illustrated in Scheme 1 below, 1,3-dicyclohexylcarbodiimide (82 mg, 0.40 mmol) was added to a solution of 3-hydroxybenzoic acid (50 mg, 0.36 mmol) and N-hydroxysuccinimide (46 mg, 0.40 mmol) in ethyl acetate (1 mL). After 1 minute, crystals of dicyclohexylurea appeared. The next day, acetic acid (20 μL) was added. The mixture was filtered through glass wool, washed with dilute HCl (1N) and dried over Na2SO4. The solution was concentrated to a white solid. Thin layer chromatography on silica gel with 1:1 ethyl acetate:hexane showed complete conversion of the starting acid to a fluorescent, lower rf product. ##STR2##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05795729 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-53b8ef1ea9a54fbb8297972007115b51 |
| Source note | uspto-grants-1998_08 |