HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-Chloro-3-nitro-5-trifluoromethylbenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-chloro-3-nitro-5-(trifluoromethyl)benzoic Acid | HCID 10084457 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Chloro-3-nitro-5-trifluoromethylbenzoyl chloride | HCID 20034167 | — |
Reaction Steps
To a solution of 2-chloro-3-nitro-5-trifluoromethylbenzoic acid (1.35 g) in toluene (15 ml) are added 1.2 ml of SOCl2. After refluxing for 2 hours, the end of the reaction is confirmed by monitoring by infrared (new band at 1788 cm−1). The reaction medium is evaporated to dryness and the resulting yellow oil, 2-chloro-3-nitro-5-trifluoromethylbenzoyl chloride, is used without further purification in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947675B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-ff50158b04b64ee09384d10d96283c6c |
| Source note | uspto-grants-2011_05 |