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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539745Generated: October 25, 2026

Nitrogen → 2-Bromo-1-[3-nitro-4-(trifluoromethyl)phenyl]ethanone

https://huagongshe.com/reaction/539745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantThionyl ChlorideHCID 24386—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant3-Nitro-4-(trifluoromethyl)benzoic acidHCID 2779015—
ReactantAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
SolventDichloromethaneHCID 6344—
Product2-Bromo-1-[3-nitro-4-(trifluoromethyl)phenyl]ethanoneHCID 5751626983%

Reaction Conditions

Temperature95 °C

Reaction Steps

3-Nitro-4-(trifluoromethyl)benzoic acid (Matrix Scientific, 2.35 g, 10 mmol) is dissolved in thionyl chloride (22 mL, 300 mmol). The stirred solution is heated at 95° C. for 16 hr, then cooled, concentrated and CH2Cl2 (51 mL) and trimethylsilyldiazomethane (20 mL, 2 M in Hexanes, 40 mmol) are added and the reaction is stirred for 2 hr at room temp. The mixture is cooled to 0° C. and HBr/HOAc (6.33 mL, 33% of HBr in HOAc) is added dropwise (N2 evolution). After addition the mixture is stirred at 0° C. for 5 min, then concentrated and purified by silica gel chromatography (CH2Cl2) to give the title compound (2.59 g, 83% yield). LCMS m/z=313.5 [M+H]+, tR=2.65 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871767B2
Source datasetuspto-grants-2014_10
ORD IDord-e5755538df574e1e83fd0aea75d7ee18
Source noteuspto-grants-2014_10