Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Methyltriphenylphosphonium iodide | HCID 638159 | — |
| Reactant | HCID 21286947 | HCID 21286947 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53841034 | HCID 53841034 | 56% |
Reaction Steps
40.4 g (0.1 moles) of methyltriphenylphosphonium iodide were suspended in 400 ml of anhydrous ether under argon gas flow. After cooling the mixture to 0° C., 90 ml (0.15 moles) of a hexane solution of n-butyl lithium were dripped. 19.6 g (0.1 moles) of 2,3-dihydro-2,3,5-trimethyl-6-(2-methyl-1-oxoethyl)-4H-pyran-4-on obtained in Example 3 were added dripwise to the mixture solution, and the mixture was agitated for 1 hour to obtain 10.1 g of 2,3-dihydro-2,3,5-trimethyl-6-(3-methyl-1-propenyl)-4H-pyran-4-one. The yield was 56%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04782168 |
|---|
| Source dataset | uspto-grants-1988_11 |
|---|
| ORD ID | ord-1a7e3155f3354008ad0691cb00cf3fac |
|---|
| Source note | uspto-grants-1988_11 |
|---|