HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Benzyl 2-(4-cyano-7-fluoro-5-methyl-6-phenylbenzoxazol-2-yl)-2-methylpropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-Amino-5-cyano-2-fluoro-6-methylbiphenyl-3-yl 2,2-dimethylmalonate | HCID 86630826 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl 2-(4-cyano-7-fluoro-5-methyl-6-phenylbenzoxazol-2-yl)-2-methylpropionate | HCID 68585926 | 856.5% |
Reaction Steps
A mixture of 4-amino-5-cyano-2-fluoro-6-methylbiphenyl-3-yl 2,2-dimethylmalonate (I-63) (500 mg, 1.12 mmol), p-toluenesulfonic acid monohydrate (21 mg, 0.112 mmol) and toluene (20 ml) was heated under reflux for 2 hours. After cooling, the reaction liquid was diluted with ethyl acetate, successively washed with an aqueous saturated sodium hydrogencarbonate solution and saturated brine, dried on anhydrous magnesium sulfate, then the solvent was evaporated away to obtain a pale brown residue. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=6:1) to obtain the entitled compound (411 mg, 86%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737166B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-01f59e144b3a4bffbcc0a62b2f70e8c6 |
| Source note | uspto-grants-2010_06 |