Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-[(4-Fluorophenyl)methyl]thiophene | HCID 10583905 | — |
| Reactant | 2-(4-Fluorobenzyl)-5-iodothiophene | HCID 10615467 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 5-(4-Fluorophenyl)-2-iodothiophene | HCID 23367310 | — |
Reaction Steps
A mixture of 2-(4-fluorobenzyl)thiophene (8.4 g, 43.7 mmol), HIO3 (1.86 g, 10.6 mmol), I2 (4.86 g, 19.2 mmol), ethyl acetate (66 ml), acetic acid (7.7 ml) and conc. H2SO4 (0.79 ml) was heated at 35° C. overnight (GC-MS showed that all the starting material is converted to 5-(4-fluorobenzyl)-2-iodothiophene). To the reaction mixture was added brine solution (33 ml), the organic layer was separated and washed with sodium hydroxide/sodium thiosulfate solution (33 ml) (prepared from 2.3 g of NaOH, 3.3 g of Na2S2O3 in 27 ml of H2O), followed by 10% of NaHCO3 solution (33 ml). The organic layer was concentrated to yield 13.9 g of 5-(4-fluorophenyl)-2-iodothiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05580989 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-ba49f26fae5847c386a7b6e0ba744788 |
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| Source note | uspto-grants-1996_12 |
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