HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 5-Bromo-3,3-dimethyl-7-hexanoyl-2,3-dihydrobenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | 5-Bromo-3,3-dimethyl-2,3-dihydro-1-benzofuran | HCID 5323595 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-3,3-dimethyl-7-hexanoyl-2,3-dihydrobenzofuran | HCID 22731298 | — |
Reaction Steps
Following General Procedure I and using aluminum chloride 1.76 g, 13.2 mmol), 20 mL of anhydrous dichloromethane, hexanoyl chloride (1.76 g, 13.2 mmol) and 5-bromo-3,3-dimethyl-2,3-dihydro-benzofuran (Intermediate 2, 1.5 g, 6.61 mmol) followed by flash column chromatography on silica gel (230-400 mesh) using 3% ethyl acetate in hexane as the eluent, the title compound was obtained as a yellow oil. It was used as such for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06720423B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-118471512ccd4bb9a9fb8f0c8d4a6837 |
| Source note | uspto-grants-2004_04 |