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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | (4aR,5R,8aR)-5-[(R)-5-Hydroxy-1,5-dimethyl-hexyl]-4a-methyl-octahydro-naphtalen-1-one | HCID 11022791 | — |
| Reactant | TMS-Imidazole | HCID 14420972 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4aR,5R,8aR)-5-[(R)-1,5-Dimethyl-5-trimethylsilanyloxy-hexyl]-4a-methyl-octahydro-naphtalen-1-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05905074 |
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| Source dataset | uspto-grants-1999_05 |
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| ORD ID | ord-7e90d3077e4945459e8b3d1087ddc67b |
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| Source note | uspto-grants-1999_05 |
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