HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (3S)-3-(tert-Butyldimethylsiloxy)-3-cyclohexylprop-1-yne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Product | (3S)-3-(tert-Butyldimethylsiloxy)-3-cyclohexylprop-1-yne | HCID 11983898 | — |
Reaction Steps
To a solution of (S)-3-cyclohexylprop-1-yn-3-ol, (obtained according to Preparation 10) (2.76 g, 0.02 mol), in 10 ml N,N-dimethylformamide (DMF), cooled to 0° C., was added imidazole (2.1 g), followed by tert-butyldimethylchlorosilane (3.1 g, 0.02 mol). The mixture was stirred for 3 h. Water (80 ml) and hexane (80 ml) were added; the organic layer was separated and combined with 2×80 ml of hexane extractions of the aqueous layer. The solvent was removed (in vacuo), after drying over sodium sulfate, to give a crude residue (4.3 g) which was chromatographed on silica gel (80 g), eluting with ethyl acetate-hexane (2:1, v/v) to afford (S)-3-tert-butyldimethylsilyloxy-3-cyclohexylprop-1-yne.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04735966 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-cce85f4917e848c489e972ae28d5ec41 |
| Source note | uspto-grants-1988_04 |