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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418390Generated: October 30, 2026

2(3H)-Benzoxazolone → HCID 59627760, compound

https://huagongshe.com/reaction/418390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2(3H)-BenzoxazoloneHCID 6043—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
Reactant5-Iodo-4'-methyl-biphenyl-3-carboxylic acid methyl esterHCID 57851588—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
ProductHCID 59627760HCID 59627760—

Reaction Conditions

Temperature110 °C

Reaction Steps

5-Iodo-4′-methyl-biphenyl-3-carboxylic acid methyl ester (200 mg, 0.57 mmol) was dissolved in DMF (3 mL) and 2-benzoxazolinone (270 mg, 2.0 mmol), K3PO4 (424 mg, 2.0 mmol), CuI (15 mg), and 1,2-bis(methylamino)cyclohexane (0.15 mL) were added. The reaction mixture was stirred at 110° C. overnight, then cooled to room temperature and partitioned between water and ethyl acetate. The organic layer was concentrated under reduced pressure and the residue was purified by preparative thin layer chromatography (3:1 hexanes/ethyl acetate) to give 4′-methyl-5-(2-oxo-benzooxazol-3-yl)-biphenyl-3-carboxylic acid methyl ester, which was used directly in the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093275B2
Source datasetuspto-grants-2012_01
ORD IDord-75728a6496b5466faed0a38bcd4dbdcd
Source noteuspto-grants-2012_01