HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 22054218, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride | HCID 10986715 | — |
| Reactant | HCID 22054289 | HCID 22054289 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22054218 | HCID 22054218 | 100% |
Reaction Steps
p-Methoxyaniline (13 mg, 0.1056 mmol), triethylamine (15 mg, 0.1485 mmol) and 2-chloro-1,3-dimethylimidazolinium chloride (24 mg, 0.1420 mmol) were added to a methylene chloride solution (3 ml) of 6-(5,6-dimethoxy-1,4-benzoquinon-2-yl)methyl-2-benzyloxybenzoic acid (29 mg, 0.0687 mmol) and the resulting solution was stirred at room temperature for 3 hours. The reaction solution was poured into ice water and then extracted with ether. The extract was washed with water and then dried, and the solvent was removed by distillation. The obtained residue was purified by preparative thin-layer chromatography (hexand:ethyl acetate=1:1) to obtain the titled compound (20 mg, 0.0687 mmol, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07064124B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-4187bf889e3847b2b45aa93a4e57d72d |
| Source note | uspto-grants-2006_06 |