HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3,4-dibutylthiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3,4-Dibromothiophene | HCID 18452 | — |
| Reactant | HCID 178418682 | HCID 178418682 | — |
| Catalyst | HCID 178418745 | HCID 178418745 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3,4-dibutylthiophene | HCID 11298534 | 64% |
Reaction Steps
Butylmagnesium bromide (140 mmol) was added dropwise at 0° C. to a mixture solution of 3,4-dibromothiophene (50 mmol) and [1,3-bis (diphenylphosphino)propane]dichloronickel(II) (0.3 mmol) in 100 mL of dry diethyl ether. The resulting mixture was heated and refluxed for 6 hours. The reaction mixture was combined with water, and extracted with diethyl ether. The extract solution was derived over magnesium sulfate, and the solvent was evaporated therefrom to obtain a crude product. The crude product was purified by silica gel column chromatography and by distillation to obtain the intended product (32 mmol) in a 64% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462726B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-de883761642c48e3a70ebd0cdb4fe557 |
| Source note | uspto-grants-2008_12 |