HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521747Generated: October 27, 2026
Iodine → 1-Iodo-4-methoxy-2-(methoxymethoxy)benzene
https://huagongshe.com/reaction/521747
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 1-Bromo-4-methoxy-2-(methoxymethoxy)benzene | HCID 14827037 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Iodo-4-methoxy-2-(methoxymethoxy)benzene | HCID 12955832 | 84% |
Reaction Steps
To a stirred solution of 2-bromo-5-methoxy-1-methoxymethoxybenzene (1.04 g, 4.23 mmol) in THF (13 mL) at −95° C. (hexanes/N2) was added n-BuLi (1.6 M in hexanes, 2.91 mL, 4.65 mmol) and the resulting solution was stirred for 5 min. To this solution was then added by syringe a solution of I2 (1.28 g, 5.07 mmol) in THF (8.5 mL) until a yellow color persisted. The solution was then permitted to warm to 23° C. and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, petroleum ether:Et2O 8:1) to provide 2-iodo-5-methoxy-1-methoxymethoxybenzene as a pale-orange oil (1.04 g, 84%). See also Tsukayama, M., 1997.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328127B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-1cc1e574176a4fcf8c277c2ba71d4f0b |
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| Source note | uspto-grants-2016_05 |
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