HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358415Generated: October 30, 2026
Nitric Acid → 1-Methyl-2-nitro-3-(trifluoromethyl)benzene
https://huagongshe.com/reaction/358415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | (Trifluoromethyl)benzene | HCID 7368 | — |
| Reactant | 3-Methylbenzotrifluoride | HCID 136246 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methyl-2-nitro-3-(trifluoromethyl)benzene | HCID 13455431 | — |
Reaction Steps
The nitration vessel is charged with 250 gms (3.97 moles) of 98% HNO3 and cooled to about -18° C. Then 100 gms (0.62 moles) of 3-methyl benzotrifluoride is added dropwise with stirring and the temperature is maintained within the range of about -16° C. to about -22° C. The addition of the benzotrifluoride takes about 2 hours and 15 minutes. After it has been added, stirring is continued for about another 15 minutes. The reaction mixture is poured into ice water and methylene chloride is added to phase separate the nitration products. The organic layer is washed with sodium carbonate solution. The solvent is then stripped on a rotary evaporator. Yield is 127.5 gms of oil comprising 43% 2-nitro isomer; 31% 4-nitro isomer, 24% 6-nitro isomer and about 1% of the 5-nitro isomer as determined by glc and 19F NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04467125 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-fa67449060fa4d18a433c2884a761326 |
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| Source note | uspto-grants-1984_08 |
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