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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197135Generated: November 1, 2026

Hydrochloric Acid → HCID 54391473, compound

https://huagongshe.com/reaction/1197135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(2-Methoxy-4-benzyloxyphenyl)pyridine-2,6-dicarboxylic acidHCID 19790322—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 54391473HCID 5439147365%

Reaction Steps

To a suspension of 10 g (0.026 mole) of the diacid 22 in 100 ml of CH2Cl2 and 7 drops of DMF was added, at 0° C., in a dropwise fashion 12 ml (0.138 mole) of oxalyl chloride. After addition the mixture was allowed to come to room temperature with vigorous evolution of HCl gas and stirred for 2 hours. The resulting homogeneous solution was then cooled in an ice bath and 20 ml of methanol in 40 ml of CH2Cl2 was slowly added. The resulting mixture was stirred for 30 minutes at room temperature and poured into 300 ml of water. The organic phase was removed, washed with 10% NaHCO3, water, dried (Na2SO4) and solvents removed. The crude diester (15 g) was purified via plug filtration with SiO2 /EtOAc/CH2Cl2 (20:80) yielding 7.0 g (65%) of the diester (23): NMR (CDCl3) 3.85 (s,3,OCH3), 4.05 (s,6,CO2Me), 5.1 (s,2,OCH2O), 6.7 and 7.4 (m,3,--C6H3O2R2) 7.35 (s,5,--C6H5), 8.5 (s,2,--C5H2N'.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116989
Source datasetuspto-grants-1992_05
ORD IDord-96916f06d1df4c328510d96b26d5a0e1
Source noteuspto-grants-1992_05