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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant3-Nitro-5-(trifluoromethyl)benzoic acidHCID 616602—
SolventMethanolHCID 887—
ProductMethyl 3-nitro-5-(trifluoromethyl)benzoateHCID 1894215793.1%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-c3848884e18b4e9e8985bb5c57ce8933
Source noteuspto-grants-2014_10