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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16506Generated: October 25, 2026

2-(4-Iodophenyl)oxazole → 2-[4-[(4-Methoxyphenyl)methyl]phenyl]oxazole

https://huagongshe.com/reaction/16506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Iodophenyl)oxazoleHCID 9860258—
ReactantHCID 178490612HCID 178490612—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product2-[4-[(4-Methoxyphenyl)methyl]phenyl]oxazoleHCID 6848894981.5%

Reaction Steps

A Schlenk Flask was charged with tetrakis(triphenylphosphine)palladium(0) (0.42 g, 0.37 mmol), nitrogen, THF (20 ML), 2-(4-iodophenyl)oxazole (1 g, 3.7 mmol), and 4-methoxybenzyl zinc chloride (0.5 M in THF, 9.6 mL, 4.8 mmol). After 3 hours, the filtrate was concentrated. The resulting solid was treated with a mixture of ethyl acetate and a dilute aqueous ammonium chloride solution. The mixture was filtered and the organic layer was dried and concentrated. Purification on silica gel using a gradient of dichloromethane in hexane gave 0.8 g of 2-[4-[(4-methoxyphenyl)methyl]phenyl]oxazole, 1H NMR (400 MHz, CDCl3) δ 7.97 (d, 2H), 7.68 (s, 1H), 7.27 (d, 2H), 7.22 (s, 1H), 7.13 (d, 2H), 6.82 (d, 2H), 3.96 (s, 2H), 3.78 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737145B2
Source datasetuspto-grants-2010_06
ORD IDord-8e049b8b96ed452eac66c484c763dd3d
Source noteuspto-grants-2010_06