HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Mercaptoethanol → 2-(6-Methyl-5-nitro-pyridin-2-ylsulfanyl)-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Fluoro-2-methyl-3-nitropyridine | HCID 12408185 | — |
| Product | 2-(6-Methyl-5-nitro-pyridin-2-ylsulfanyl)-ethanol | HCID 11424429 | 105.6% |
Reaction Steps
To a solution of 2-fluoro-5-nitro-6-picoline (5.0 g, 32 mmol) and 2-mercaptoethanol (4.5 ml, 64 mmol), KOH (2 g, 36 mmol) was added at 0° C. The mixture was stirred at the same temperature for 15 minutes. The crude mixture was extracted with AcOEt and brine. Organic phase was dried over MgSO4, filtered, and concentrated to provide the crude 2-(6-methyl-5-nitro-pyridin-2-ylsulfanyl)-ethanol as an oil (7.238 g). 1HNMR (DMSO-d4, 400 MHz) δ 2.75 (s, 3H), 3.30-3.33 (m, 2H), 3.63-3.67 (m, 2H), 4.65-4.68 (m, 1H), 7.40-7.43 (m, 1H), 8.24-8.26 (m, 1H). Exact mass calculated for C8H10N2O3S 214.04 found 215.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362248B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-926251e159964bfb9cf7106e716fbe20 |
| Source note | uspto-grants-2013_01 |