HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534837Generated: October 29, 2026
Acetyl chloride → Methyl 3-nitro-5-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/534837
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-Nitro-5-(trifluoromethyl)benzoic acid | HCID 616602 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-nitro-5-(trifluoromethyl)benzoate | HCID 18942157 | 93.1% |
Reaction Steps
To an ice cooled stirred solution of 3-nitro-5-(trifluoromethyl)benzoic acid (25.00 g, 106.3 mmol) in methanol (500 mL) was added acetyl chloride (22.00 g, 280.2 mmol) dropwise over 20 min. After the addition was complete, the reaction mixture was stirred for 20 min at 0° C., then heated at reflux for 6 h and then cooled to room temperature. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in ethyl acetate, washed with saturated aqueous sodium bicarbonate, filtered through a silica gel and concentrated under reduced pressure to provide methyl 3-nitro-5-(trifluoromethyl)benzoate (24.65 g, 93%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853215B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c3848884e18b4e9e8985bb5c57ce8933 |
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| Source note | uspto-grants-2014_10 |
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