HuagongsheHuagongshe Chemistry Print Report · For research reference only
Naphthalene → 1-(1-Methylethyl)naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | P-Cymene | HCID 7463 | — |
| Product | 1-(1-Methylethyl)naphthalene | HCID 22535 | — |
Reaction Steps
Reaction was carried out similarly as in Example 11, but using p-cymene to transalkylate naphthalene. Yield of isopropylnaphthalene obtained was 21%, with 90% β- and 10% α-isopropylnaphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04288646 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-9ec41ac167904cc0832b6b3ca148db89 |
| Source note | uspto-grants-1981_09 |