HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-chloro-3-nitro-5-trifluoromethylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Chloro-3-nitro-5-trifluoromethylbenzoyl chloride | HCID 20034167 | — |
| Product | Ethyl 2-chloro-3-nitro-5-trifluoromethylbenzoate | HCID 67200596 | — |
Reaction Steps
The 2-chloro-3-nitro-5-trifluoromethylbenzoyl chloride (5.5 g; 18 mmol), obtained in step b) of Example 1, is dissolved in ethanol (50 ml) and stirred for 1 hour at room temperature. After evaporating to dryness, the pasty solid is purified by filtration on silica (eluent: dichloromethane). 4.2 g of ethyl 2-chloro-3-nitro-5-trifluoromethylbenzoate are obtained in the form of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947675B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-4ce5ae9eb8cb4074b6c19af214c5d9bf |
| Source note | uspto-grants-2011_05 |