HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-dihydro-2H-pyran → 1-Heptadecene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Carboxyhexacyclo[6.6.1.13,6.110,13.02,7.09,14]heptadecen | HCID 86755175 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Heptadecene | HCID 23217 | — |
Reaction Steps
Subsequently, carboxyhexacyclo[6.6.1.13,6.110,13.02,7.09,14 ]heptadecen of 2.1 grams and 3,4-dihydro-2H-pyran of 1.71 grams were dissolved in tetrahydrofuran of 50 milli-litter, and p-toluen sulfonic acid of 0.03 gram was added to the solution. The reaction was continued at room temperature for 2 hours. The resultant material was diluted in ether of 100 milli-litter, and was washed in 3% solution of Na2CO3, saturated water of salt and water in this order, and the organic layer was dried with MgSO4. When ether and residual 3,4-dihydro-2H-pyran were removed in vacuum by using an evaporator, we obtained viscous-liquid of 12-tetrahydropyranyloxycarbonilhexacyclo[6.6.1.13,6.110,13.02,7.09,14 ]heptadecen of 2 grams.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06030747 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-b097b090a3c541ebbc2a013b8f37936f |
| Source note | uspto-grants-2000_02 |