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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518134Generated: November 1, 2026

Hydrochloric Acid → HCID 71532156, compound

https://huagongshe.com/reaction/518134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Aminosalicylic AcidHCID 4649—
ReactantEthyl formateHCID 8025—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantSodium ethoxideHCID 2723922—
Reactant209796-27-0HCID 18628861—
ReactantEthanol hydrochlorideHCID 21887872—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventEthylene GlycolHCID 174—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 71532156HCID 7153215632%

Reaction Steps

To a solution of 2-(3-bromothiophen-2-yl)acetonitrile (1.0 g) and ethyl formate (3.7 g) in dimethyl sulfoxide (5.0 mL) was added sodium ethoxide (20% solution in ethanol, 3.1 mL), and the mixture was stirred at room temperature for 3 hours. 2.5 mol/L hydrochloric acid ethanol solution (3.6 mL) and 4-amino-2-hydroxybenzoic acid (0.9 g) were added to reaction solution. The mixture was stirred at 50° C. for 5 hours. To the reaction solution was added water. The precipitated solid was collected by filtration, washed with water, and dried under reduced pressure at 50° C. for 3 hours. The obtained residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=87/13−78/22) to give the condensate (0.91 g). To a solution of this condensate (0.91 g) in dimethyl sulfoxide (4.5 mL) were added copper(I) iodide (47 mg), ethylene glycol (0.3 g) and tripotassium phosphate (1.1 g), and the mixture was stirred at 80° C. for 5 hours. After cooling to 50° C., to the mixture was added 2 mol/L hydrochloric acid (8.7 mL) and the mixture was stirred at room temperature for 1 hour. The precipitated solid was collected by filtration, washed with mixed solution of water and dimethyl sulfoxide, 1 mol/L hydrochloric acid and water, and dried under reduced pressure at 50° C. to give the title compound (0.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115144B2
Source datasetuspto-grants-2015_08
ORD IDord-91feb121955143cc810162568358f0bd
Source noteuspto-grants-2015_08