HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 10476669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 85966947 | HCID 85966947 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 10476669 | HCID 10476669 | 65% |
Reaction Steps
Intermediate 63 (0.2 g, 0.62 mM) was dissolved in 40 ml of chloroform. To it was added p-anisidine (0.21 g, 1.66 mM), 0.19 g triethylamine and the reaction was refluxed for 18 hrs. Solvent was evaporated and the residue was extracted in ethyl acetate. The organic layer was washed with 10% HCl solution, brine and then dried over anhydrous Na2SO4. It was then evaporated to obtain the crude residue which was then purified over silica gel column using ethylacetate-hexane system to obtain the desired compound as beige solid with a yield of 65% (0.16 g); mp 190-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238725B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-9be862be32d44b87b62f562413e2d3c1 |
| Source note | uspto-grants-2007_07 |