Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437033Generated: November 1, 2026

Methyl Salicylate → HCID 57485433, compound

https://huagongshe.com/reaction/1437033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl SalicylateHCID 4133—
ReactantCesium carbonateHCID 10796—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium DithioniteHCID 24489—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-1-fluoro-2-nitrobenzeneHCID 2736328—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 57485433HCID 574854339%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of a methyl 2-hydroxybenzoate (1.0 mL, 10.0 mmol), 5-bromo-2-fluoronitrobenzene (0.62 mL, 5.0 mmol) and Cs2CO3 (3.3 g, 10.0 mol) in DMF (12 mL) was stirred at 40° C. for 2 h. The mixture was diluted with EtOAc and washed with 2 M aqueous NaOH-solution. To the EtOAc-phase was added EtOH, H2O, K2CO3 (2.8 g, 20 mmol) and Na2S2O4 (3.5 g, 20 mmol) and the resulting mixture was stirred vigorously for 1 h. The aqueous phase was removed and the organic phase was washed with 1 M aqueous NaOH-solution and then concentrated. The residue was taken up in DMF (1 mL) and then toluene (4 mL) and NaH (60 mg, 1.5 mmol, 60% in mineral oil) were added and the resulting mixture was stirred at 80° C. over night, then quenched by addition of saturated aqueous NH4Cl-solution. The resulting mixture was diluted with EtOAc, washed with 2 M aqueous NaOH-solution, dried (Na2SO4), concentrated, filtered through a short SiO2-column, concentrated and crystallised from heptane:EtoAc to give 130 mg of the title compound (189JO56). MS (ESI) 290 (MH+). Purity for MH+ (UV/MS) 100/100.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622461B2
Source datasetuspto-grants-2009_11
ORD IDord-44493a735f1f440c8f452dc8ec64311a
Source noteuspto-grants-2009_11