Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739360Generated: October 31, 2026

Ethanol → 1,2-Bis(4-bromophenyl)-2-hydroxyethanone

https://huagongshe.com/reaction/1739360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
Reactant4-BromobenzaldehydeHCID 70741—
Catalyst3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromideHCID 9964923—
Product1,2-Bis(4-bromophenyl)-2-hydroxyethanoneHCID 3938243100%

Reaction Steps

A solution of 4-bromobenzaldehyde (25.0 g, 0.135 mol), 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide (1.70 g, 0.0068 mol) and triethylamine (4.10 g, 0.0405 mol) in ethanol (125 mL) is stirred at room temperature for 60 hours. The reaction mixture is concentrated to dryness, then taken up in CH2Cl2 (150 mL), washed with 1 M HCl and saturated aqueous NaHCO3 and dried (Na2SO4), then concentrated, giving 25.2 g (100 percent) of a viscous yellow oil which solidifies upon standing at room temperature. 1H NMR (CDCl3) δ 7.73 (d, J=8.5 Hz, 2H), δ7.52 (d, J=8.5 Hz, 2H), 7.44 (d, J=8.2 Hz, 2H), 7.17 (d, J=8.2 Hz, 2H) 13C NMR (CDCl3) δ 197.33, 137.56, 132.33, 132.13, 131.90, 130.43, 129.46, 129.31, 122.93, 75.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965679
Source datasetuspto-grants-1999_10
ORD IDord-7cf0864fef8e4d3999f77b965635226a
Source noteuspto-grants-1999_10