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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13778Generated: October 25, 2026

Isopropyl Acetate → 4-(Bromomethyl)-3-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/13778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl AcetateHCID 7915—
Reactant4-Methyl-3-(trifluoromethyl)benzoic acidHCID 2775592—
ReactantSodium BisulfiteHCID 23665763—
ReactantSodium BromateHCID 23668195—
SolventWaterHCID 962—
Product4-(Bromomethyl)-3-(trifluoromethyl)benzoic acidHCID 2314589360.1%

Reaction Steps

To 60.0 g of 4-methyl-3-trifluoromethylbenzoic acid was added 600 ml of isopropyl acetate. Under stirring at room temperature, a solution of 133.0 g of sodium bromate in 420 ml of water and a solution of 91.7 g of sodium hydrogensulfite in 180 ml of water were added in turn. The mixture was gradually heated from 30° C. up to 50° C. at intervals of 10° C. and stirred until the color of the reaction solution disappeared. The aqueous layer was separated to remove, and to the organic layer were added a solution of 133.0 g of sodium bromate in 420 ml of water and a solution of 91.7 g of sodium hydrogensulfite in 180 ml of water, and then the mixture was gradually heated up to 60° C. as above. After separation, to the organic layer were further added a solution of 133.0 g of sodium bromate in 420 ml of water and a solution of 91.7 g of sodium hydrogensulfite in 180 ml of water, and the mixture was gradually heated as above and heated to the temperature the mixture was finally refluxed. After the completion of the reaction, the reaction solution was separated, the organic layer was washed twice with a 5% aqueous sodium thiosulfate solution and twice with 15% saline, dried over anhydrous magnesium sulfate, and, then the solvent was distilled off under reduced pressure. To the residue was added 120 ml of n-heptane, the mixture was stirred, and then the crystals were collected by filtration to obtain 50.0 g of the objective compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728131B2
Source datasetuspto-grants-2010_06
ORD IDord-d4435aab212941fdaa4e2f6e47c96c09
Source noteuspto-grants-2010_06