HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 3-Benzo[1,3]dioxol-5-yl-5-hydroxy-N-phenyl-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | 3-Benzo[1,3]dioxol-5-yl-5-benzyloxy-benzoic Acid | HCID 57905834 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Benzo[1,3]dioxol-5-yl-5-hydroxy-N-phenyl-benzamide | HCID 57905867 | 76% |
Reaction Steps
3-Benzo[1,3]dioxol-5-yl-5-benzyloxy-benzoic acid (500 mg), PyBroP (1.2 eq.), aniline (1.1 eq.), and triethylamine (2 eq.) were combined in dichloromethane (5 mL) and stirred at room temperature overnight. The reaction mixture was diluted with dichloromethane and washed with water. White solid which precipitated in dichloromethane layer was collected by filtration (493 mg). This material was dissolved in THF and hydrogenated over 10% Pd/C (50 mg) in Parr apparatus for 5 h. The catalyst was removed by filtration and the filtrate was concentrated under reduced pressure and purified on a silica gel column using ethyl acetate and hexanes to yield 362 mg of title compound (76% yield after 2 steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989454B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-e7aea721b56a427791b3393124945344 |
| Source note | uspto-grants-2011_08 |