HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662458Generated: November 1, 2026
Sodium Iodide → 2'-Fluoro-2-(1-hydroxy-2,2-dimethyl-but-3-enyl)-5'-methoxy-biphenyl-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/1662458
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-Butene, 1-bromo-3-methyl- | HCID 70092 | — |
| Reactant | Indium | HCID 5359967 | — |
| Reactant | 2'-Fluoro-2-formyl-5'-methoxy-biphenyl-4-carboxylic acid methyl ester | HCID 57467630 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2'-Fluoro-2-(1-hydroxy-2,2-dimethyl-but-3-enyl)-5'-methoxy-biphenyl-4-carboxylic acid methyl ester | HCID 57467632 | 94% |
Reaction Steps
To a mixture of 66.60C (0.38 g, 1.3 mmol), 1-bromo-3-methylbut-2-ene (commercially available from Aldrich) (0.31 mL, 2.6 mmol) and sodium iodide (0.40 g, 2.6 mmol) in DMF (8 mL), was added indium (0.30 g, 2.6 mmol). The resulting mixture was stirred at room temperature for 1 hour and then additional 1-bromo-3-methylbut-2-ene (100 mg) and indium (100 mg) were added and the mixture was stirred at room temperature for one more hour. The reaction was quenched with water (20 mL) and extracted with EtOAc (200 mL). The organic phase was washed with brine, dried over anhydrous sodium sulfate, and filtered. After removing solvent, the residue was purified by flash chromatography (silica gel, 1:4 EtOAc/hexane) and gave product (66.60D), in 94% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030354B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-17a720b28d1b4ca8b4022651c38c9ea8 |
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| Source note | uspto-grants-2011_10 |
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