HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butyl nitrite → Ethyl 5-phenylthiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | ethyl 2-amino-5-phenylthiophene-3-carboxylate | HCID 638860 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | Ethyl 5-phenylthiophene-3-carboxylate | HCID 58110324 | 73.4% |
Reaction Steps
Anhydrous copper (II) chloride (4 g, 0.03 mol) and tert-butyl nitrite (1.9 mL, 0.019 mol) were dissolved in IMS (100 mL) then treated with 2-amino-5-phenyl-thiophene-3-carboxylic acid ethyl ester (2 g, 8.097 mmol). After 30 minutes saturated aqueous ammonium chloride (20 mL) was added and the mixture left for a further 30 minutes. The resultant precipitate was filtered off and the filtrate was concentrated, washed with DCM, dried and concentrated to give a dark oil which was purified by column chromatography, eluting with 0-35% tert-butyl methyl ether in cyclohexane to afford 5-phenyl-thiophene-3-carboxylic acid ethyl ester as a yellow oil (1.38 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08614209B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-45f921380f6f41569b9950dd09a98e32 |
| Source note | uspto-grants-2013_12 |