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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449803Generated: October 29, 2026

1-Propanol → Methyl 4-(2-chloro-5-methylpyrimidin-4-yl)-2-methoxybenzoate

https://huagongshe.com/reaction/449803

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PropanolHCID 1031—
ReactantPyrimidine, 2,4-dichloro-5-methyl-HCID 74508—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 22171502—
SolventTolueneHCID 1140—
ProductMethyl 4-(2-chloro-5-methylpyrimidin-4-yl)-2-methoxybenzoateHCID 8664381556.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 2,4-dichloro-5-methylpyrimidine (244 mg, 1.5 mmol) and methyl 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (210 mg, 1.0 mmol) in toluene (3 mL) were added n-propanol (1 mL), aqueous sodium bicarbonate (2 M, 1.5 μL) and tetrakis(triphenylphosphine)palladium[0] (116 mg, 0.1 mmol). The reaction was heated at 110° C. for 40 h, then partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The aqueous layer was extracted twice further with ethyl acetate and the combined organic fractions were washed with water, brine then dried (sodium sulfate), filtered and concentrated. Silica gel chromatography using 30-60% ethyl acetate/petroleum spirit as eluent provided methyl 4-(2-chloro-5-methylpyrimidin-4-yl)-2-methoxybenzoate as a cream solid (165 mg, 56%); LC-ESI-MS (method B): rt 6.2 min.; m/z 293.3/295.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486941B2
Source datasetuspto-grants-2013_07
ORD IDord-2e114b481fcb4ba58870680cfa99b50d
Source noteuspto-grants-2013_07