Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741202Generated: October 30, 2026

Ethanethiol → 2-(4-Hydroxyphenyl)-3-[4-[2-(piperidin-1-yl)ethoxy]benzoyl]-6-hydroxybenzofuran

https://huagongshe.com/reaction/1741202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 9891548HCID 9891548—
Solvent1,2-DichloroethaneHCID 11—
Product2-(4-Hydroxyphenyl)-3-[4-[2-(piperidin-1-yl)ethoxy]benzoyl]-6-hydroxybenzofuranHCID 9955756—

Reaction Steps

The title product was prepared by the demethylation of 2-(4-methoxyphenyl)-3-[4-[2-(piperidin-1-yl)ethoxy]benzoyl]-6-methoxybenzofuran, the product of Example 1a, supra. In a 250 ml three-neck round bottom flask were combined ethylene chloride (50 ml) and aluminum trichloride (9.60 g, 72 mmol) and ethanethiol (6.39 g, 103 mmol) to create a pale yellow liquid. To this liquid was then added the product of Example la (5.00 g, 10.3 mmol) in a gradual fashion. A red oil precipitated and the mixture was stirred for about 20 minutes. After cooling the reaction mixture in an ice bath 100 ml of tetrahydrofuran was added and the mixture was allowed to stir until all of the oil had gone into solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972888
Source datasetuspto-grants-1999_10
ORD IDord-eb290794d8e1432689b6b2b3b8c0768d
Source noteuspto-grants-1999_10