HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 4-[(4-Fluorophenyl)methyl]-2-iodothiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 3-(4-Fluorophenylmethyl)thiophene | HCID 19963302 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[(4-Fluorophenyl)methyl]-2-iodothiophene | HCID 21184084 | 87.6% |
Reaction Steps
To a solution of LDA (3.67 mmol) in THF at -78° C. was added a solution of 3-(4-fluorophenylmethyl)thiophene (640 mg, 3.33 mmol), prepared as in Example 35, step 1, and the reaction mixture was stirred for 25 min. A solution of I2 (1.01 g, 4.00 mmol) in THF was added and the cold bath was removed. The reaction mixture was warmed to ambient temperature, quenched with saturated aqueous NH4Cl, and extracted with ether. 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 to give 928 mg of 2-iodo-4-(4-fluorophenylmethyl)thiophene which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616596 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-cb52e8c476aa46659077dc04a3cff3df |
| Source note | uspto-grants-1997_04 |