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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713672Generated: November 1, 2026

Sodium Carbonate → 2-(3-Thiophen-3-yl-phenyl)-ethanol

https://huagongshe.com/reaction/1713672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantThiophene-3-boronic acidHCID 581760—
Reactant2-(3-Bromophenyl)ethan-1-olHCID 2734090—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-(3-Thiophen-3-yl-phenyl)-ethanolHCID 19917133—

Reaction Steps

A mixture of 3-bromo-phenethyl-alcohol (1 g, 4.97 mmol), 3-thiophene-boronic-acid (1.9 g, 14.9 mmol, 3.0 equiv), Pd(PPh3)4 (172 mg, 0.149 mmol, 0.03 equiv), and 2M Na2CO3 (10.8 mL, 22.4 mmol, 4.5 equiv) in toluene (40 mL) is heated to reflux 1 h, under an argon atmosphere. The resulting suspension is allowed to cool to RT and filtered through a pad of celite, washing the filter cake with CH2Cl2 and water. The layers are separated. The organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. Purification of the crude material by silica gel column chromatography (CH2Cl2/Et2O, 95/5) affords the title compound: ES-MS: 205.0 [M+H]+; single peak at tR=4.27 min (System 2); Rf=0.32 (CH2Cl2/Et2O, 95/5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795288B2
Source datasetuspto-grants-2010_09
ORD IDord-c333d8530e324d0e887d6deebcdbac7a
Source noteuspto-grants-2010_09