Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3,3-Dimethyl-1-butyne | HCID 13512 | — |
| Reactant | 2-(3-Bromopropoxy)tetrahydro-2H-pyran | HCID 2777988 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19917043 | HCID 19917043 | 40.7% |
Reaction Steps
0.81 g of tert-butylacetylene was dissolved in 19 ml of tetrahydrofuran, and 6.1 ml of a 0.55M n-butyllithium-hexane solution was added dropwise with stirring at -78° C. After the mixture was stirred at this temperature for 1 hour, 2.2 g of 3-bromo-1-(2-tetrahydropyranyloxy)propane was added. The solution was warmed to the room temperature, and then heated at 80° C. with stirring for 8 hours. The reaction mixture was poured into the ice water, and ethyl ether was added. The organic layer separated was worked up in a customary manner, and the product was purified by silica gel column chromatography [hexane / ethyl acetate=20 /1] to give 0.90 g of 6,6-dimethyl-1-(2-tetrahydropyranyloxy)-4-heptyne.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05306728 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-0259fb1e56df4f8686c1b8d27ae392a1 |
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| Source note | uspto-grants-1994_04 |
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