HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069260Generated: October 31, 2026
Methanol → Methyl 2-amino-5-nitro-4-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/2069260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Amino-5-nitro-4-trifluoromethyl-benzoic acid | HCID 18536731 | — |
| Product | Methyl 2-amino-5-nitro-4-(trifluoromethyl)benzoate | HCID 11965778 | 90% |
Reaction Steps
A solution of 28 g (112 mmol) of 2-amino-5-nitro-4-trifluoromethyl-benzoic acid in 550 ml of methanol is cooled to 0° C. under nitrogen and concentrated H2SO4 is added dropwise in order to keep the temperature around 20° C. Upon completion of the addition, the mixture is heated to reflux for 24 hours. It is then allowed to cool to room temperature and the mixture is concentrated in vacuo to about 50 ml. This residue is poured onto ice and extracted with ethyl acetate. The organic phase is washed with a saturated aqueous solution of NaHCO3 and brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product is recrystallized in toluene to give 26.7 g (90%) of 2-amino-5-nitro-4-trifluoromethyl-benzoic acid methyl ester as yellow crystals, m.p. 174-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08299085B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-78be601b9a8e42fa8d9b1c945c99f8c7 |
|---|
| Source note | uspto-grants-2012_10 |
|---|