Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271015Generated: October 30, 2026

Pyridine → HCID 18387761, compound

https://huagongshe.com/reaction/2271015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Thiophen-2-ylphenolHCID 3564197—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18387761HCID 1838776179.5%

Reaction Steps

To a mixture of 4-(2-thienyl)phenol (1.00 g) and acetic anhydride (869 mg) in tetrahydrofuran (10 ml) was added pyridine (494 mg) with ice-cooling. The mixture was stirred for 1 hour at said temperature and 1 hour at ambient temperature. After concentration, the mixture was partitioned between AcOEt and H2O. The separated organic layer was washed with 1% aqueous citric acid, 3% aqueous NaHCO3 solution and brine, dried over sodium sulfate and concentrated. The residue was triturated with hexane to give 985 mg of 2-(4-acetoxyphenyl)thiophene as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333324B1
Source datasetuspto-grants-2001_12
ORD IDord-bd1ad6567ac44e729bc3b7b0944527a2
Source noteuspto-grants-2001_12