HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 66580148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | (2S)-1,1,1-Trifluoropropan-2-ol | HCID 6999971 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66580148 | HCID 66580148 | — |
Reaction Steps
In a 4-neck flask, commercially available 2-chloro-5-nitropyridine (71.9 g) and (S)-1,1,1-trifluoropropan-2-ol (54.3 g) were dissolved in DMF (610 ml) and sodium hydride (20 g, 55%) was added at a temperature of 16 to 18° C. (ice cooling). Following addition, the mixture was allowed to stir for 1 hour. The mixture was poured into ice and was allowed to hydrolyze. The suspension was warmed to RT over a period of 12 hours and the solid was filtered and washed with additional water and then with a small amount of hexanes (50 mL). The brown solid was further dried in vacuo to provide the title compound. (81.9 g). 1H-NMR (δ, CDCl3): 9.06 (m, 1H), 8.43 (dd, 1H), 6.93 (d, 1H), 5.87 (m, 1H); 1.54 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08703807B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-a7fa1ed80f644a5fbf57a9fe1a3ef8ae |
| Source note | uspto-grants-2014_04 |