HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 3-nitro-2-piperid-1-yl-5-trifluoromethylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Ethyl 2-chloro-3-nitro-5-trifluoromethylbenzoate | HCID 67200596 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 3-nitro-2-piperid-1-yl-5-trifluoromethylbenzoate | HCID 67201256 | — |
Reaction Steps
To a solution of ethyl 2-chloro-3-nitro-5-trifluoromethylbenzoate (4.2 g; 1 eq.) in dioxane (40 ml) is added piperidine (3.9 ml; 2.1 eq.). After stirring for 18 hours at room temperature, the medium is poured into water (50 ml) and the product is extracted with ethyl ether. The organic phase is washed with water, dried and concentrated. 4.9 g of ethyl 3-nitro-2-piperid-1-yl-5-trifluoromethylbenzoate are obtained in the form of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947675B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-a48ea0c23a7e491d84c7b2ec039d713f |
| Source note | uspto-grants-2011_05 |