HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethoxyethane → Ethyl 5-chloro-2-(quinolin-6-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Quinolin-6-ylboronic Acid (contains varying amounts of Anhydride) | HCID 4192671 | — |
| Reactant | Ethyl 5-chloro-2-iodobenzoate | HCID 51341862 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 5-chloro-2-(quinolin-6-yl)benzoate | HCID 67253873 | 39.1% |
Reaction Steps
A degassed mixture of ethyl 5-chloro-2-iodobenzoate (0.621 g, 2.00 mmol), Pd(PPh3)4 (0.116 mg, 0.1 mmol), quinolin-6-ylboronic acid (0.381 g, 2.2 mmol), K2CO3 (0.553 g, 4.0 mmol), dimethoxyethane (20 mL), and water (5 mL) was heated under reflux overnight. Solvents were removed under reduced pressure. The residue was diluted with sat'd NH4Cl (15 mL) and extracted with EtOAc (3×30 mL). The combined organic layers were dried (MgSO4), concentrated in vacuo and purified by chromatography to afford ethyl 5-chloro-2-(quinolin-6-yl)benzoate (0.244 g, 39% yield) as a colorless oil. MS (ESI) m/z: 312.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790756B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-cd8ff515f9ee4738a323a883ab234c98 |
| Source note | uspto-grants-2010_09 |