HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cuminaldehyde → HCID 20543003, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cuminaldehyde | HCID 326 | — |
| Reactant | Triphenyl(1-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethyl)phosphonium bromide | HCID 11238302 | — |
| Product | HCID 20543003 | HCID 20543003 | — |
Reaction Steps
In a manner analogous to that described in Example 1, from [1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)ethyl]-triphenylphosphonium bromide and 4-isopropyl-benzaldehyde there can be obtained 6-[(E)-p-isopropyl-α-methylstyryl]-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene of melting point 86°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04326055 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-725c9517fb75465694ae3acf8af8bf5e |
| Source note | uspto-grants-1982_04 |