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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075558Generated: October 25, 2026

Imidazole → (4aR,5R,8aR)-5-[(R)-1,5-Dimethyl-5-trimethylsilanyloxy-hexyl]-4a-methyl-octahydro-naphtalen-1-one

https://huagongshe.com/reaction/1075558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant(4aR,5R,8aR)-5-[(R)-5-Hydroxy-1,5-dimethyl-hexyl]-4a-methyl-octahydro-naphtalen-1-oneHCID 11022791—
ReactantTMS-ImidazoleHCID 14420972—
SolventTetrahydrofuranHCID 8028—
Product(4aR,5R,8aR)-5-[(R)-1,5-Dimethyl-5-trimethylsilanyloxy-hexyl]-4a-methyl-octahydro-naphtalen-1-oneHCID 70273562—

Reaction Steps

A solution of 24 mg (0.08 mMol) of (4aR,5R,8aR)-5-[(R)-5-Hydroxy-1,5-dimethyl-hexyl]-4a-methyl-octahydro-naphtalen-1-one in 0.5 ml of tetrahydrofuran is cooled under stirring and Argon atmosphere to 0°. The reaction mixture is stirred for an additional hour after addition of 12 μl (0.08 mMol) of trimethylsilylimidazole, of 5.1 μl (0.04 mMol) of trimethylsilylchloride and of 2.8 mg (0.04 mMol) of imidazole. The reaction mixture is poured into ice water, extracted three times with diethylether, the combined organic extracts are washed twice with brine and dried over Na2SO4. The organic solvent is evaporated in vacuo and the residue is chromatographed over 5 g of silicagel with hexane/diethylether 9/1 to yield 25 mg of pure, oily (4aR,5R,8aR)-5-[(R)-1,5-Dimethyl-5-trimethylsilanyloxy-hexyl]-4a-methyl -octahydro-naphtalen-1-one

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05905074
Source datasetuspto-grants-1999_05
ORD IDord-7e90d3077e4945459e8b3d1087ddc67b
Source noteuspto-grants-1999_05