HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → n-(4-Methoxyphenyl)-2-(4-tert-butylbenzoyloxy)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-tert-Butylbenzoyl chloride | HCID 74372 | — |
| Reactant | N-(4-Methoxyphenyl)-2-hydroxybenzamide | HCID 478806 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | n-(4-Methoxyphenyl)-2-(4-tert-butylbenzoyloxy)benzamide | HCID 18174417 | 61% |
Reaction Steps
To a solution of N-(4-methoxyphenyl)-2-hydroxybenzamide (0.484 g, 2.00 mmol) in methylene chloride (35 mL) cooled to 0° C. was added 0.28 mL triethylamine (0.28 mL, 2.0 mmol), followed by the dropwise addition of a solution of 4-tert-butylbenzoyl chloride (0.393 mL, 2.00 mmol) in methylene chloride (15 mL). The reaction mixture was allowed to warm to room temperature over 16 h and washed with cold water. The organic layer was dried (magnesium sulfate), filtered, and concentrated in vacuo. Trituration with hexane provided 0.488 g (61%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313122B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-1d68e6b8ab8f45a9b1fa7d5183e1ca76 |
| Source note | uspto-grants-2001_11 |