HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 2-anilino-5-phenylthiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | ethyl 2-amino-5-phenylthiophene-3-carboxylate | HCID 638860 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-anilino-5-phenylthiophene-3-carboxylate | HCID 58256479 | — |
Reaction Steps
A vial was charged with copper acetate (77 mg, 0.425 mmol), ethyl 2-amino-5-phenylthiophene-3-carboxylate (100 mg, 0.404 mmol), phenylboronic acid (99 mg, 0.809 mmol), dichloromethane (2 ml), and triethylamine (0.113 ml, 0.809 mmol). The blue-green reaction mixture was magnetically stirred for 19 hours and then concentrated to a volume of 0.5 mL. The crude reaction mixture was purified by silica gel chromatography (7-60% dichloromethane/hexanes) to afford ethyl 2-anilino-5-phenylthiophene-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420695B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-617977799adc4f2cb87484740037c563 |
| Source note | uspto-grants-2013_04 |