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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418533Generated: November 2, 2026

Methanol → HCID 53747526, compound

https://huagongshe.com/reaction/1418533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantHCID 53929149HCID 53929149—
Catalyst1,3-Bis(diphenylphosphino)propaneHCID 81219—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 53747526HCID 53747526—

Reaction Conditions

Temperature70 °C

Reaction Steps

2-Fluoro-5-methoxy-4-propylphenyl triflate (3.00 g, 9.5 mmol), triethylamine (2.91 mL, 20.9 mmol) and methanol (7.0 mL, 173 mmol) were dissolved in DMF (30 mL) and the solution was flushed with CO. 1,3-Bis(diphenylphosphino)propane (151 mg, 0.37 mmol) and palladium-acetate (84 mg, 0.37 mmol) were added and the reaction was stirred at 70° C. and atmospheric pressure for 4.5 h. Evaporation of the solvent and co-evaporation with xylene gave a residue which was extracted between Et2O and 2M NaOH and the organic phase was washed brine, dryed over MgSO4 and evaporated to give 2.3 g of crude product. Purification by flash chromatography (SiO2, CH2Cl2 -hexane 1:2) gave methyl 2-fluoro-5-methoxy-4-propylbenzoate (1.46 g) as an oil. 1H NMR (DMSO-d6): δ 7.28 (d, J=6.0 Hz, 1 H), 7.12 (d, J=11.4 Hz, 1 H), 3.83 (s, 3 H), 3.80 (s, 3 H), 2.54 (t, J=7.6 Hz, 2 H), 1.53 (m, J=7.6 Hz, 2 H), 0.87 (t, J=7.4 Hz, 3 H). 13C NMR (DMSO-d6): δ 164.01 (d, J=4 Hz), 155.21 (d, J=251 Hz), 152.95, 138.30 (d, J=8 Hz), 117.93 (d, J=24 Hz), 115.26 (d, J=11 Hz), 111.75, 55.88, 52.20, 31.32, 21.83, 13.66. MS (EI, 70 eV): m/z (rel.int) 226 (M+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883129
Source datasetuspto-grants-1999_03
ORD IDord-4e75fb1be9f740bb910155657343a866
Source noteuspto-grants-1999_03