HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → Ethyl 3-(7-bromo-2,3-dihydro-1-benzofuran-5-yl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Ethyl 3-(2,3-dihydrobenzofuran-5-yl)propanoate | HCID 11053175 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 3-(7-bromo-2,3-dihydro-1-benzofuran-5-yl)propanoate | HCID 10891878 | 97.5% |
Reaction Steps
Bromine (10.5 g, 65.8 mmols) was dropwise added to an acetic acid (150 ml) solution containing ethyl 3-(2,3-dihydrobenzofuran-5-yl)propionate (14.5 g, 65.8 mmols) and sodium acetate (5.94 g, 72.4 mmols), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. Water was added to the residue, which was then extracted with ethyl acetate. The extract was washed with a saturated saline solution and then dried with anhydrous magnesium sulfate. This was concentrated under reduced pressure to obtain 19.2 g (yield: 97%) of the target compound. This was oily.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218429B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-34afec7ce78f41ecbe5033eeb6c46bf8 |
| Source note | uspto-grants-2001_04 |