HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,2-Trifluoroethanol → 3-Nitro-5-sulphamyl-4-(beta,beta,beta-trifluoroethoxy)-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | 4-Chloro-3-nitro-5-sulphamoylbenzoic acid | HCID 89893 | — |
| Product | 3-Nitro-5-sulphamyl-4-(beta,beta,beta-trifluoroethoxy)-benzoic acid | HCID 21505991 | — |
Reaction Steps
To a solution of sodium β, β, β -trifluoroethoxide in β, β, β-trifluoroethanol (prepared by dissolving 2.1 g of sodium in 45 ml of β ,β ,β-trifluoroethanol), 4-chloro-3-nitro-5-sulphamyl-benzoic acid (4.2 g) was added, and the resulting solution was refluxed for 5 days. After evaporation of the reaction mixture in vacuo, water (50 ml) was added, and the aqueous solution was acidified with 4N hydrochloric acid. After standing in a refrigerator, the precipitate was collected by suction. After several recrystallizations from aqueous ethanol, the 3-nitro-5-sulphamyl-4-(β ,β ,β-trifluoroethoxy)-benzoic acid was obtained with a melting point of 195°-197°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03971819 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-58ba6232f7034438adf3ade7dcc87e35 |
| Source note | uspto-grants-1976_07 |