HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Aminophenylacetic acid ethyl ester → ethyl[4-(4,9-diethoxy-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Aminophenylacetic acid ethyl ester | HCID 225219 | — |
| Reactant | 2,3-Bis(bromomethyl)-1,4-diethoxy-naphthalene | HCID 21079334 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl[4-(4,9-diethoxy-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate | HCID 131726211 | 36% |
Reaction Steps
A solution of 2,3-bis(bromomethyl)-1,4-diethoxy-naphthalene (41 mg, 0.1 mmol) and 4-aminophenylacetic acid ethyl ester (20 mg, 0.11 mmol) in N,N-dimethylformamide (1 ml) was heated at 60° C. under nitrogen for 14 h. The solvent was removed in vacuo and the residue taken up in ethyl acetate (10 ml) and washed with 8% aqueous sodium bicarbonate solution (5 ml). The organic layer was dried over magnesium sulphate and the solvent removed in vacuo. Purification by flash column chromatography on silica gel eluting with 90% cyclohexane/ethyl acetate gave the product as a white solid (15 mg, 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732622B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-053c8e8e62434c409462a28dcbd344c3 |
| Source note | uspto-grants-2010_06 |