HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638187Generated: November 1, 2026
Imidazole → (S)-1,3-Di-[(tert-butyldimethylsilyloxy)]-4-methyl-4-pentene
https://huagongshe.com/reaction/1638187
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | (S)-1-[(tert-butyldimethylsilyloxy)]-4-methyl-4-penten-3-ol | HCID 10966327 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-1,3-Di-[(tert-butyldimethylsilyloxy)]-4-methyl-4-pentene | HCID 11336893 | 98% |
Reaction Steps
946 mg (6.28 mmol, 1.3 equivalents) of tert-butyldimethylchlorosilane is added to a solution of 1.173 g (4.83 mmol) of (S)-1-[(tert-butyldimethylsilyloxy)]-4-methyl-4-penten-3-ol 10and 855 mg (12.56 mmol, 2.6 equivalents) of imidazole in 15.0 ml of absolute DMF. The mixture is stirred for 16 hours at room temperature. It is mixed with 50 ml of an aqueous 1 M KHSO4 solution and extracted four times with 50 ml of Et2O each. The combined ether extracts are dried on MgSO4. After the solvent is distilled off in a vacuum, the residue is flash-chromatographed by a silica gel column with pentane/Et2O (20:1). As an alternative to this aqueous working-up, the reaction mixture can be chromatographed directly. By the two variations of working-up procedure, 1.643 g (4.73 mmol, 98%) of 11 is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06043372 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-905789b17a984f1d8ccc6a4c8875a2ef |
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| Source note | uspto-grants-2000_03 |
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