HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diallyl ether → HCID 14484952, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diallyl ether | HCID 11194 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | HCID 14484952 | HCID 14484952 | — |
Reaction Steps
In a manner analogous to that described above for 2a, 36 (1.00 g, 6.66 mmol) was alkylated with allyl bromide (1.76 g, 14.6 mmol) to give the allyl ether. The allyl ether (1.23 g) was thermally rearranged in 1,2-dichlorobenzene (8 mL) at 190° C. for 3.5 hours to afford, after chromatographic purification, compound 37. Recrystallization from hexane gave an analytical sample. 37: mp 60°-61° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04966907 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-a794759b2b9b41bcab4f12211500743e |
| Source note | uspto-grants-1990_10 |