HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418390Generated: October 30, 2026
2(3H)-Benzoxazolone → HCID 59627760, compound
https://huagongshe.com/reaction/418390
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2(3H)-Benzoxazolone | HCID 6043 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-N,2-N-dimethylcyclohexane-1,2-diamine | HCID 551074 | — |
| Reactant | 5-Iodo-4'-methyl-biphenyl-3-carboxylic acid methyl ester | HCID 57851588 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59627760 | HCID 59627760 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093275B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-75728a6496b5466faed0a38bcd4dbdcd |
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| Source note | uspto-grants-2012_01 |
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