Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Triethylsilyl trifluoromethanesulphonate | HCID 2733308 | — |
| Reactant | HCID 54058176 | HCID 54058176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54297662 | HCID 54297662 | 95% |
Reaction Steps
A mixture of (S)-5,5-dimethyl-1-hexyn-4-ol (1.96 g 16 mmol), triethylamine (4.5 ml, 32 mmol) and dry dichloromethane (30 ml) was cooled to 0° C. under a nitrogen atmosphere. Triethylsilyl trifluoromethanesulphonate (5.4 ml, 24 mmol) was slowly added and the mixture stirred at 0° C. for a further 40 min. The mixture was treated with saturated sodium bicarbonate solution (60 ml) and the organic layer separated. The aqueous layer was extracted with dichloromethane (3×20 ml) and the combined dichloromethane extracts dried (MgSO4) and evaporated. The residue was purified by column chromatorgaphy (silica eluted with Petroleum ether 40-60°) to yield the title compound 3.55 g (95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962659 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-54dbc43218124fccba0b2e8b8b8e0039 |
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| Source note | uspto-grants-1999_10 |
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