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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745530Generated: October 26, 2026

Hydrochloric Acid → 2-(3-thienyl)benzaldehyde

https://huagongshe.com/reaction/745530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantN,N-dimethyl-4-nitrosoanilineHCID 8749—
ReactantSodium HydroxideHCID 14798—
Reactant3-[2-(Bromomethyl)phenyl]thiopheneHCID 13552993—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product2-(3-thienyl)benzaldehydeHCID 4321315—

Reaction Steps

To a solution of Compound 2b (1.98 mmol) in chloroform (5 mL) was added pyridine (9.88 mmol) and the reaction mixture heated at reflux for 1 hour under nitrogen. The solvent was removed in vacuo and the residue triturated with diethyl ether to give a white solid. The solid was dissolved in 95% aqueous ethanol (10 mL ) and N,N-dimethyl-4-nitrosoaniline (1.98 mmol) was added with stirring followed by the addition of sodium hydroxide (4.0 mmol) in water (3 mL). The reaction mixture was stirred for 16 hours at ambient temperature and then 6N hydrochloric acid (3 mL) was added. After 30 minutes, the solvent was removed in vacuo and the residue was diluted with water (10 mL) and extracted with diethyl ether (2×30 mL). The combined organic phases were washed with saturated aqueous sodium bicarbonate, brine and the solvent removed in vacuo to give crude Compound 2c as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04599341
Source datasetuspto-grants-1986_07
ORD IDord-c307eb18a9c64f08bbb10f86adf65512
Source noteuspto-grants-1986_07