Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantPotassium bisulfateHCID 516920—
Reactant(S)-1-[(tert-butyldimethylsilyloxy)]-4-methyl-4-penten-3-olHCID 10966327—
SolventDimethylformamideHCID 6228—
Product(S)-1,3-Di-[(tert-butyldimethylsilyloxy)]-4-methyl-4-penteneHCID 1133689398%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043372
Source datasetuspto-grants-2000_03
ORD IDord-905789b17a984f1d8ccc6a4c8875a2ef
Source noteuspto-grants-2000_03