HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Ethoxy-5-nitro-1,3-bis(trifluoromethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Chloro-5-nitro-1,3-bis(trifluoromethyl)benzene | HCID 11300854 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Ethoxy-5-nitro-1,3-bis(trifluoromethyl)benzene | HCID 86666595 | 96.7% |
Reaction Steps
Ethanol (20 mL, 343 mmol) was treated with potassium hydroxide (956 mg, 17.0 mmol) and the mixture was stirred at RT for 1 h. A solution of 2-chloro-5-nitro-1,3-bis(trifluoromethyl)benzene (1) (1.00 g, 3.41 mmol) in DMSO (10 mL) was added dropwise. The resultant mixture was stirred at RT for 1 h. The mixture was partitioned between EtOAc and water and the aqueous phase was extracted twice with EtOAc. The combined organic phases were washed with brine, dried over MgSO4, filtered and the solvent removed in vacuo to afford 2-ethoxy-5-nitro-1,3-bis(trifluoromethyl)benzene (2) (1.00 g, 93%) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ: 8.72 (2H, s), 4.21 (2H, q), 1.41 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447028B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-74e0c5cb1e9943aa826529780e22bf7a |
| Source note | uspto-grants-2016_09 |