Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 4-Bromoanisole | HCID 7730 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-2-iodo-1-methoxybenzene | HCID 10979904 | — |
Reaction Steps
4-Bromo-anisole (4.417 g, 23.6 mmol) was dissolved in acetonitrile (200 mL) and placed under an argon atmosphere in the absence of light. Iodobenzene diacetate (9.18 g, 28.5 mmol) was added followed by iodine (3.6 g, 14.2 mmol). The mixture was stirred for 16 hours at ambient temperature. The mixture was then poured into 1M Na2S2O3 (200 mL) and stirred until the solution was colourless. The solution was then extracted with diethyl ether (3×100 mL). The combined organic extracts were then washed with brine, dried with Na2SO4, filtered and evaporated to dryness. The crude product was filtered through a silica gel plug eluting with heptane/ethyl acetate (3:1) (200 mL). The filtrate was concentrated and the residue was distilled using a Kugelrohr apparatus collecting the compound at 75° C., 0.01 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612068B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-86dd5d4d1e75444d9e018dbf24cbbe0c |
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| Source note | uspto-grants-2009_11 |
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