HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722366Generated: October 29, 2026
Imidazole → (5-Chloro-1-pentyloxy)(2,2-dimethylethyl)dimethylsilane
https://huagongshe.com/reaction/1722366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 5-Chloro-1-pentanol | HCID 78915 | — |
| Solvent | Water | HCID 962 | — |
| Product | (5-Chloro-1-pentyloxy)(2,2-dimethylethyl)dimethylsilane | HCID 20028701 | — |
Reaction Steps
5-Chloropentanol (325 g, 2.65 moles) is added to a solution containing tert-butyldimethylsilyl chloride (439 g, 2.91 moles) and dimethylformamide (1.625 liters). The solution is stirred and imidazole (199 g, 2.91 moles) is added at once. The solution is stirred at room temperature for 6 hours, after which time water (1 liter) is added and the reaction is partitioned with hexanes. The organic phase is separated and the solvent volume reduced under vacuum. The residue is dried over anhydrous magnesium sulfate and the remaining solvent removed under vacuum, leaving a clear, colorless oil. The crude product is subsequently fractionally distilled under reduced pressure leaving the product as a clear, colorless oil (534 g, 2.26 moles), BP 71° C./0.3 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04855322 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-ec93d5375f7b4828b6fa9483421a2b2a |
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| Source note | uspto-grants-1989_08 |
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