HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396217Generated: October 29, 2026
Sulfuric Acid → 3-Chloro-5-nitrobenzotrifluoride
https://huagongshe.com/reaction/396217
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Chloro-6-nitro-4-(trifluoromethyl)aniline | HCID 2734081 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Chloro-5-nitrobenzotrifluoride | HCID 50255 | — |
Reaction Steps
(see also: EP 0 516 297 A1) 56.7 ml of 96% sulfuric acid are added dropwise over a period of 30 minutes to a brown solution of 90 g (374 mmol) of 4-amino-3-chloro-5-nitro-benzotrifluoride (Maybridge; Tintagel/England) in 500 ml of ethanol (exothermic). After heating to 75° C., 64.53 g (935 mmol) of sodium nitrite are added in portions over a period of one hour (evolution of gas). The mixture is stirred for 2.5 hours at 75° C. and then cooled to room temperature. The reaction mixture is poured onto 1.5 liters of ice-water and extracted four times with ether. Washing the organic phases with 0.1 N HCl, saturated NaHCO3solution and brine, drying (Na2SO4) and concentration by evaporation yield a brown oil. Column chromatography (SiO2; hexane) yields the title compound in the form of an oil: 1H-NMR (DMSO-d6) 8.62 (m, 1H), 8.46 (m, 2H), MS 225 (M)+, 179 (M—NO2)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608071B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-49feda6b86c84729a658ab84827da99a |
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| Source note | uspto-grants-2003_08 |
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