HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → 5-Ortho-tolylpentene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Product | 5-Ortho-tolylpentene | HCID 10877425 | — |
Reaction Steps
The synthesis of 2,6-NDC typically includes several steps. In a typical synthesis, orthoxylene and butadiene are reacted over an alkali metal or other catalyst to yield a 5-orthotolylpentene (5-OTP) alkenylation product. The 5-OTP is then cyclized over an acid catalyst to yield 1,5 dimethyltetralin (1,5-DMT). The 1,5 DMT is dehydrogenated over a noble metal or some other dehydrogenation catalyst to yield 1,5-dimethylnaphthalene(1,5-DMN), which is subsequently isomerized to produce 2,6-dimethylnaphthalene (2,6-DMN).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06495710B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-0bb272cfd1554fd1b9a940863f0e1439 |
| Source note | uspto-grants-2002_12 |