Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552293Generated: October 31, 2026

3,5-Dimethyl-4-hydroxybenzaldehyde → 1-(5-Ethyl-4-p-tolyl-thiophen-2-yl)-3-(4-hydroxy-3,5-dimethyl-phenyl)-propan-1-one

https://huagongshe.com/reaction/552293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dimethyl-4-hydroxybenzaldehydeHCID 75222—
Reactant1-(5-Ethyl-4-p-tolyl-thiophen-2-yl)-ethanoneHCID 67166307—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product1-(5-Ethyl-4-p-tolyl-thiophen-2-yl)-3-(4-hydroxy-3,5-dimethyl-phenyl)-propan-1-oneHCID 59248992105.7%

Reaction Steps

A solution of 1-(5-ethyl-4-p-tolyl-thiophen-2-yl)-ethanone (28 mg, 0.115 mmol) and 3,5-dimethyl-4-hydroxybenzaldehyde (26 mg, 0.172 mmol) in ethanol (1.5 mL) and 5 N HCl in isopropanol (0.3 mL) is stirred at rt for 18 h. The solution is diluted with water and extracted with EA. The organic extract is evaporated, dissolved in methanol (3 mL) and THF (3 mL) and treated with Pd/C (30 mg, 10% Pd). The slurry is stirred under 1.5 bar of H2 for 18 h. The mixture is filtered, the solvent of the filtrate is removed in vacuo and the crude product is purified by prep. HPLC to give 1-(5-ethyl-4-p-tolyl-thiophen-2-yl)-3-(4-hydroxy-3,5-dimethyl-phenyl)-propan-1-one (46 mg) as a colourless oil; LC-MS: tR=1.13 min, [M+1]+=379.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951794B2
Source datasetuspto-grants-2011_05
ORD IDord-aad9c69b0d7b4d698e683df1e79cc9c3
Source noteuspto-grants-2011_05