HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 7-fluoro-4-methoxy-1-benzothiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | 2,3-Difluoro-6-methoxybenzaldehyde | HCID 2774112 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 7-fluoro-4-methoxy-1-benzothiophene-2-carboxylate | HCID 22171205 | 87.4% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
Methyl thioglycolate (28.8 mL, 320 mmol) was added under nitrogen to a solution of triethylamine (86.6 mL) in dry NN-dimethylformamide (220 mL) at 80° C. Stirred at 100° C. for 15 mins. A solution of 2,3-difluoro-6-methoxybenzaldehyde (55.1 g, 320 mmol) in N,N-dimethylformamide (80mL) was added and the mixture heated at 130° C. for 3h. Allowed to cool then poured onto ice-water (2L). The resulting yellow solid was filtered, washing with water (2×200 mL). Dried under vacuum over phosphorus pentoxide at room temperature overnight to give the title compound (67.2 g, 87%); δH (300 MHz, CDCl3) 8.20 (1H, d, ArH), 7.06 (1H, t, ArH), 6.68 (1H, m, ArH) and 3.99 (6H, s, OCH3 and CO2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07417064B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-d641117e9b6b4753b50bd436db0ae9a2 |
| Source note | uspto-grants-2008_08 |