HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 4,5-Dibromo-1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 3-(6,7-dibromo-2,3-dihydrobenzofuran-5-yl)propanoic Acid | HCID 11024537 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4,5-Dibromo-1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-one | HCID 11727281 | 89% |
Reaction Steps
A mixture of 3-(6,7-dibromo-2,3-dihydrobenzofuran-5-yl)propionic acid (10.0 g, 28.6 mmols), dichloromethane (35 mL), thionyl chloride (5.11 g, 40.8 mmols) and N,N-dimethylformamide (30 mg) was heated to reflux for 1 hour. After cooling, aluminum chloride (4.66 g, 43.3 mmols) was added to the reaction mixture a trot more than 0° C. and then the mixture was stirred for 30 min. The reaction mixture was poured into precooled methanol (200 mL), then stirred for 30 min. Crystals precipitated were collected by filtration, washed with water (500 mL) followed by methanol (500 mL) to obtain 7.9 g (yield: 89%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06348485B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-48d5da54d39348e8b7e85b4cdf353cf7 |
| Source note | uspto-grants-2002_02 |