HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387668Generated: October 31, 2026
Imidazole → Tert-butyl[4-(iodomethyl)phenoxy]dimethylsilane
https://huagongshe.com/reaction/2387668
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (4-((Tert-butyldimethylsilyl)oxy)phenyl)methanol | HCID 10014460 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl[4-(iodomethyl)phenoxy]dimethylsilane | HCID 21760231 | 41% |
Reaction Steps
Triphenyl phosphine (1.32 g, 5.03 mmol), imidazole (370 mg, 5.47 mmol) and iodine (1.16 g, 4.61 mmol) were added to an ice-cooled solution of 4-(tert-butyldimethylsilyloxy)benzyl alcohol [(1 g, 4.19 mmol), Tet. Lett. (2004), 45, 9617] in tetrahydrofuran (50 mL) and the mixture was stirred at 0° C. for 10 minutes and room temperature for 30 minutes. The reaction mixture was then concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was separated, dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentane, afforded the title compound in 41% yield, 600 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268881B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-fb03a50cdcef4c07a11a5985894d3d7c |
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| Source note | uspto-grants-2012_09 |
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