HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965340Generated: October 26, 2026
Sodium Iodide → 1-(Tert-butyldimethylsilyl)oxy-3-iodocyclohexane
https://huagongshe.com/reaction/965340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-(Tert-butyldimethylsilyl)oxy-1-(methylsulfonyloxy)cyclohexane | HCID 22629252 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Tert-butyldimethylsilyl)oxy-3-iodocyclohexane | HCID 22629188 | — |
Reaction Steps
A solution of 3-(tert-butyldimethylsilyl)oxy-1-(methylsulfonyloxy)cyclohexane (15.9 g) and sodium iodide (8.5 g) in N,N-dimethylformamide (80 ml) was heated at 100° C. for 3 hours with stirring. After cooled to ambient temperature, a reaction mixture was poured into a mixture of ethyl acetate (250 ml) and n-hexane (150 ml), and insoluble material was removed by filtration. Mother liquor was washed in turn with water (100 ml×3), 5% sodium thiosulfate in water (50 ml), and saturated sodium chloride in water (100 ml×2), and dried over magnesium sulfate. Evaporation of the solvent gave a residue, which was chromatographed on silica gel (300 ml) eluting with 10% ethyl acetate in n-hexane to give 3-(tert-butyldimethylsilyl)oxy-1-iodocyclohexane (cis and trans mixture).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773530 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-589509dc8a8148a9b9a29bd2061bd16e |
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| Source note | uspto-grants-1998_06 |
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