HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Acetic acid 4-acetyl-2-(4-tert-butylphenyl)thiophen-3-yl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-t-Butylphenyl)-3-hydroxy-4-methylcarbonylthiophene | HCID 44207289 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Acetic acid 4-acetyl-2-(4-tert-butylphenyl)thiophen-3-yl ester | HCID 67050465 | 92.3% |
Reaction Steps
To a solution of 2-(4-tert-butylphenyl)-3-hydroxy-4-methylcarbonylthiophene (137 mg, 0.5 mmol) in THF (2 mL) were added triethylamine (105 μL, 0.75 mmol) and acetyl chloride (53.3 μL, 0.75 mmol). The reaction mixture was stirred at room temperature for 0.5 h. After removing solvent, the residue was diluted with AcOEt, washed with a saturated aqueous NH4Cl solution, dried over MgSO4 and concentrated to give product as a brown oil (146 mg, yield 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576115B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-84c5f9169fb546d88930ee5b86336374 |
| Source note | uspto-grants-2009_08 |