HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylhydroxamic Acid → HCID 178518983, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylhydroxamic Acid | HCID 66644 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178518983 | HCID 178518983 | 54% |
Reaction Steps
To a solution of salicylhydroxamic acid (1.53 g, 10 mmol) in THF (40 ml) was added a solution of carbonyldiimidazole (1.62 g, 20 mmol) in tetrahydrofuran (20 ml). The mixture was stirred at reflux for 4 hrs. before evaporation to dryness. Water (20 ml) and conc. HCl (aq.) (5 ml) were added and the solution was refrigerated (5° C.) for 30 min. The resulting precipitate was collected by filtration and washed with 2M HCl. The solid material was dissolved in methanol and concentrated in vacuo yielding 725 mg (54%) of the title compound 71. TLC (10% methanol in DCM): Rf=0.2. HPLC-MS (Method A): M+=136.1 (UV/MS(%)=94/100). 1H-NMR (400 MHz, CDCl3, MeOD): δ=7.73 (1H, m); 7.56 (1H, m); 7.38 (1H, m); 7.28 (1H, m); 3.87 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238713B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-247c532ac1564a71bbf72373153a7681 |
| Source note | uspto-grants-2007_07 |