HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891037Generated: October 30, 2026
Imidazole → 4-((Tert-butyldimethylsilyl)oxy)but-2-yn-1-ol
https://huagongshe.com/reaction/891037
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Butyn-1-ol | HCID 12991 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-((Tert-butyldimethylsilyl)oxy)but-2-yn-1-ol | HCID 5461845 | — |
Reaction Steps
A solution of 175 g of tert-butyldimethylsilyl chloride in 100 ml of a 1:1 mixture that consists of hexane and dimethylformamide is slowly added in drops at 0° C. under nitrogen to a solution of 100 g of 2-butin-1-ol and 158 g of imidazole in 300 ml of dimethylformamide, and it is stirred for 2 hours at 0° C. and for 16 hours at 22° C. The reaction mixture is diluted with 2.5 l of ether, washed once with water, once with 5% sulfuric acid, once with water, once with saturated sodium bicarbonate solution and washed neutral with semi-saturated sodium chloride solution. After drying on sodium sulfate and filtration, it is concentrated by evaporation in a vacuum. The residue that is thus obtained is purified by chromatography on silica gel. With hexane/0–40% ether, 74.3 g of the title compound is obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001916B1 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-5ab7c7dd027846f3b88a090e622a767a |
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| Source note | uspto-grants-2006_02 |
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