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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348276Generated: October 26, 2026

Sodium Carbonate → 2-(4-Thiophen-2-yl-phenyl)-5-methyl-4-oxazoleethanol

https://huagongshe.com/reaction/348276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactant2-(2-(4-Bromophenyl)-5-methyloxazol-4-YL)ethanolHCID 10880530—
Catalystpalladium(II) acetateHCID 167845—
Solvent1-PropanolHCID 1031—
Product2-(4-Thiophen-2-yl-phenyl)-5-methyl-4-oxazoleethanolHCID 21084283—

Reaction Steps

2-(4-Bromophenyl)-5-methyl-4-oxazoleethanol (10.0 g, 35.0 mmol) (see Ex. 1, Part G) and 2-thiophenyl boronic acid (38.0 mmol) were dissolved in n-propanol (120 ml) before adding triphenylphosphine (165.2 mg, 0.63 mmol), palladium acetate (46 mg, 2.1 mmol), and Na2CO3 (4.5 g, 42 mmol dissolved in 30 mL distilled H2O). The solution was heated to reflux and stirred for 1.5 h. After cooling to ambient temperature, the mixture was concentrated under reduced pressure and then partitioned between CH2Cl2 (100 mL) and 1N NaOH (100 mL). The aqueous phase was extracted with CH2Cl2 (2×50 mL) and the combined organic phases were dried (MgSO4) and concentrated under reduced pressure to provide 2-(4-thiophen-2-yl-phenyl)-5-methyl-4-oxazoleethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176224B2
Source datasetuspto-grants-2007_02
ORD IDord-0e73865833f949b8aab027a622d371b5
Source noteuspto-grants-2007_02