HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanol, 1-((trimethylsilyl)ethynyl)- → 1-Ethynylcyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanol, 1-((trimethylsilyl)ethynyl)- | HCID 205445 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Ethynylcyclohexanol | HCID 6525 | — |
Reaction Steps
Dissolve 1-(2-trimethylsilyl-1-ethynyl)cyclohexanol (1.79 g, 9.13 mmol) in tetrahydrofuran (11 mL) and place under an argon atmosphere. Add, by dropwise addition, tetra-n-butylammonium fluoride (11 mL of a 1M solution in tetrahydrofuran, 11 mmol). Stir for 1 hour at room temperature and partition between methylene chloride and water. Separate the organic phase, wash with saturated aqueous sodium chloride, dry (MgSO4), filter and evaporate the solvent in vacuo to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05157167 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-9407aa3917b1401fb09b205273d463da |
| Source note | uspto-grants-1992_10 |