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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488064Generated: October 25, 2026

Hydrochloric Acid → 2-(1,3-Dioxolan-2-yl)ethyl 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoate

https://huagongshe.com/reaction/488064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant2-(2-Bromoethyl)-1,3-dioxolaneHCID 87776—
Reactant2-((4,6-Dimethoxypyrimidin-2-yl)oxy)benzoic acidHCID 184185—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product2-(1,3-Dioxolan-2-yl)ethyl 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoateHCID 1527823763.8%

Reaction Steps

10 Milliliters of N,N-dimethylformamide in which 0.22 g of 60% sodium hydride in oil has been suspended was mixed with 5 ml of N,N-dimethylformamide solution of 1.38 g of 2-(4,6-dimethoxypyrimidin-2-yl)oxy benzoic acid. After stirring the mixture at room temperature for 30 minutes, 10 ml of N,N-dimethylformamide solution of 1.81 g of 2-(2-bromoethyl)-1,3-dioxolane was added thereto. The resulting solution was stirred at 100° to 110° C. for 2 hours. The reaction solution was allowed to cool, poured into diluted hydrochloric acid, and extracted with ethyl acetate. The organic layer separated from the aqueous layer was washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue obtained was subjected to silica gel column chromatography (mfd. by Merck & Co., Inc., solvent: chloroform) to obtain 1.20 g of 2-(1,3-dioxolan-2-yl)ethyl 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoate [present compound (V-2)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298632
Source datasetuspto-grants-1994_03
ORD IDord-57289cd2ff5e490b8cb79b1e767d633f
Source noteuspto-grants-1994_03