HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 15514362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | HCID 12873106 | HCID 12873106 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15514362 | HCID 15514362 | — |
Reaction Steps
2-methyl-4-(4-nitrophenyl)oxazole (J. Heteocyclic Chemistry, 1981, 885)(1.12 g, 5.48 mmol) was added to a refluxing solution of SnCl2.2H2O (6.33 g, 28.1 mmol), conc HCL (10 mL) and EtOH (20 mL). The reaction is stirred for 30 min then cooled to room temperature and poured into a solution of 24 g of KOH in 100 mL of water. The resulting mixture was cooled in an ice bath and stirred for an additional 30 min. The product was collected by filtration as a yellow solid (1.35 g, 83%). LC-MS (M+H): 191
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174949B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-c4a09259f7bd460eb7181373a7463ca0 |
| Source note | uspto-grants-2015_11 |