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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203323Generated: October 31, 2026

Methyl 2-Bromo-5-chlorobenzoate → HCID 46856402, compound

https://huagongshe.com/reaction/2203323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-Bromo-5-chlorobenzoateHCID 280500—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4,4,4-Trifluorobutanoic acidHCID 2777085—
SolventTetrahydrofuranHCID 8028—
ProductHCID 46856402HCID 46856402—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A THF solution of sodium bis(trimethylsilyl)amide (1.0M, 194 mL, 194 mmol) was added dropwise to a −78° C. THF (400 mL) solution containing methyl 2-bromo-5-chlorobenzoate (16.10 g, 64.5 mmol) and 4,4,4-trifluorobutyric acid (9.17 g, 64.5 mmol). After stirring for 15 minutes at −78° C. the solution was warmed to 0° C. and stirred for an additional 2 hours. The reaction was quenched with an excess of aqueous 1N HCl (ca 400 mL) and stirred overnight at room temperature. The solution was concentrated to remove the majority of the THF. The solution was then diluted with EtOAc and washed with 1N NaHCO3 (twice) and brine. The organic phase was then dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography using a hexanes/EtOAc gradient to give the indicated compound (solid). 1H NMR (500 MHz, CDCl3): δ 7.58 (d, J=8.4 Hz, 1H); 7.41 (d, J=2.5 Hz, 1H); 7.33 (dd, J=8.5, 2.5 Hz, 1H); 3.22 (t, J=7.8 Hz, 2H); 2.68-2.56 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365574B2
Source datasetuspto-grants-2016_06
ORD IDord-d5d1dc20aa974f8682ae9d291f9d24af
Source noteuspto-grants-2016_06