Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butylbenzene | HCID 7705 | — |
| Reactant | Pentylbenzene | HCID 10864 | — |
| Product | Naphthalene | HCID 931 | — |
| Product | 1-Methylnaphthalene | HCID 7002 | — |
Reaction Steps
Cyclodehydrogenation was carried out in the same way as Example 1 except that n-amylbenzene (a reagent produced by Tokyo Kasei K.K., purity: 98.9%) was used in place of n-butylbenzene, and that it was gasified in a nitrogen stream and introduced into the catalyst layer maintained at 550° C., at LHSV of 0.085. The conversion ratio of n-amylbenzene was 95.5%. Also, 1-methylnaphthalene was obtained at a selectivity of 72.1%, while naphthalene was obtained at a selectivity of 11.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05382733 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-bc96e0f53e69412482de4a0234dba8d8 |
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| Source note | uspto-grants-1995_01 |
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