HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362397Generated: October 29, 2026
2-Iodophenol → 1-Iodo-2-((3-methylbut-2-en-1-yl)oxy)benzene
https://huagongshe.com/reaction/1362397
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Iodophenol | HCID 10784 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Butene, 1-bromo-3-methyl- | HCID 70092 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Iodo-2-((3-methylbut-2-en-1-yl)oxy)benzene | HCID 11108961 | 98.8% |
Reaction Steps
To a solution of 2-iodophenol (3.69 g, 16.8 mmol) in THF (50 mL) is added NaH (804 mg, 33.5 mmol) portion wise and stirred for 30 min at room temperature. 3,3-Dimethylallylbromide (3.9 mL, 33.5 mmol) was added and the reaction was stirred over night at room temperature. The reaction is quenched with water (20 mL) and extracted with diethyl ether (3×25 mL), the organic layers are dried over magnesium sulfate, filtered and concentrated. The compound was purified on silica gel using 100% hexanes as the eluent to yield 4.78 g (98%) of the title compound as a pale yellow oil: 1H NMR (300 MHz, CDCl3) δ 7.77 (d, J=6.0 Hz, 1H), 7.35 (t, J=9.0 Hz, 1H), 7.02 (d, J=9.0 Hz, 1H), 6.74 (t, J=9.0 Hz, 1H), 5.45 (m, 1H), 4.60 (d, J=6.0 Hz, 2H), 1.75 (2s, 6H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879872B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-05efec81932244c4a285e40de1e6e998 |
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| Source note | uspto-grants-2011_02 |
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