HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Iodo-3-(4fluorophenylmethyl)thiophene → 2-Methyl-3-(4-fluorophenylmethyl)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Iodo-3-(4fluorophenylmethyl)thiophene | HCID 19963279 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Catalyst | HCID 178418745 | HCID 178418745 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Methyl-3-(4-fluorophenylmethyl)thiophene | HCID 19963270 | 48% |
Reaction Steps
The 2-iodo-3-(4-fluorophenylmethyl)thiophene prepared in step 1 was taken up in ether and methylmagnesium bromide (3.0M in ether, 2.42 mL, 7.26 mmol) and dichloro [1,3-bis(diphenylphosphino)propane]nickel(II) (164 mg, 0.302 mmol) were added and the reaction mixture was stirred for 17 hours at ambient temperature. The reaction mixture was quenched with saturated aqueous NH4Cl and extracted with ethyl acetate. The organic phase was washed with 1N aqueous H3PO4, saturated aqueous NaHCO3, saturated aqueous Na2S2O3, and brine, dried over MgSO4, filtered, and concentrated in vacuo. Chromatography on silica gel (10% ethyl acetate/hexane) gave 2-methyl-3-(4-fluorophenylmethyl)thiophene (602 mg, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616596 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-b9357db81ccf486c92cf642395755be2 |
| Source note | uspto-grants-1997_04 |