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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591126Generated: October 30, 2026

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

https://huagongshe.com/reaction/591126

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 numberUS09238628B2
Source datasetuspto-grants-2016_01
ORD IDord-22b8c07521bc4ce7b49ff0c74518356d
Source noteuspto-grants-2016_01