HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168055Generated: October 29, 2026
Imidazole → (S)-4-tert-butyldimethylsilyloxy-1-trityloxy-2-butanol
https://huagongshe.com/reaction/1168055
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (S)-1-trityloxy-2,4-butanediol | HCID 14027585 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-4-tert-butyldimethylsilyloxy-1-trityloxy-2-butanol | HCID 12114686 | 270.2% |
Reaction Steps
(S)-1-Trityloxy-2,4-butanediol (1.64 g, 4.7 mmol) and imidazole (0.321 g, 4.715 mmol) were dissolved in DMF (20 ml) and the solution was cooled to 0° C. To the solution was dropped tert-butyldimethylsilyl chloride (0.5 ml, 1.44 mmol, 50% in toluene). After stirring for 1 hour, again to the solution was dropped tert-butyldimethylsilyl chloride (0.5 ml, 1.44 mmol) and the solution was stirred for 1 hour. Further tert-butyldimethylsilyl chloride (0.6 ml, 1.73 mmol) was added to the solution and the solution was stirred over night at room temperature. After dilution with toluene (100 ml), the solution was washed with water (100 ml) twice and saturated brine once, dried on magnesium sulfate, filtered and condensed in vacuo. The residue was subjected to silica gel chromatography to give (S)-4-tert-butyldimethylsilyloxy-1-trityloxy-2-butanol (1.80 g, yield 82.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620977B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-d3834080934048c7b841f232f72039d1 |
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| Source note | uspto-grants-2003_09 |
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