HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopropane → Ethyl 5-bromo-3-methyl-4-[(propan-2-yl)oxy]-1-benzofuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester | HCID 12542970 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 5-bromo-3-methyl-4-[(propan-2-yl)oxy]-1-benzofuran-2-carboxylate | HCID 53428887 | 100% |
Reaction Steps
To 0.50 g (1.7 mmole) of ethyl 5-bromo-4-hydroxy-3-methyl-1-benzofuran-2-carboxylate (Example 119, Step 1) in 7 mL DMF was added 0.51 g (3.75 mmole) of potassium carbonate and 0.48 mL (3 mmole) of 2-bromopropane and the reaction was stirred at room temperature overnight. The solvent was concentrated in vacuo, and the residue was extracted with ethyl acetate and water. The organic layer washed with water and brine, dried over sodium sulfate, filtered, and concentrated to provide 0.58 g of ethyl 5-bromo-4-isopropoxy-3-methyl-1-benzofuran-2-carboxylate. Yield: 100%; m.p. 48-50° C.; MS: 341.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07420001B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-62a3dcf3a45e48b883368175bcb8307f |
| Source note | uspto-grants-2008_09 |