HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 86627417, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86627418 | HCID 86627418 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86627417 | HCID 86627417 | — |
Reaction Steps
4-(2-Aminoethoxy)-2-(2-bromobenzyloxy)benzaldehyde (200 mg, 0.43 mmol) was dissolved in CH2Cl2 (20 ml) and Et3N (87.02 mg, 0.12 ml, 0.86 mmol) was added to the solution, followed by stirring for 2˜3 min. Benzoyl chloride (60.45 mg, 50 μl, 0.43 mmol) was also added before additionally stirring at room temperature for 2 hours. After completion of the reaction, the reaction solution was extracted with brine and CH2Cl2 (×3). The organic layer was dried over anhydrous MgSO4 and filtered. The filtrate was concentrated in a vacuum. The residue was purified using column chromatography (ethyl acetate/n-hexane=1/5→1/3) to afford the object compound (white solid, 78 mg, 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08148541B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-fe14dd9cf995435f827a2ee6df78eca7 |
| Source note | uspto-grants-2012_04 |