HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexadecane → Linalool
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexadecane | HCID 11006 | — |
| Reactant | Silica | HCID 24261 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 53868284 | HCID 53868284 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Linalool | HCID 6549 | — |
Reaction Steps
A mixture of 1,5-dimethylcyclooct-1-en-5-ol (prepared as in Example II (b) 100, cyclohexane and n-hexadecane in the volume ratio 1:2:1 was passed at a rate of 12 ml/hour together with nitrogen gas at one 1/hour through a 30 cm quartz glass tube filled with 3 mm sodium glass beads at 540° C. It was shown by GLC that under these conditions the conversion of starting material was 39% and the selectivity to the required product was 87%. The alpha-linalool was recovered by distillation b.p. 91°-92° C. at 20 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04214098 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-489feb032798442389a50dbe48273e98 |
| Source note | uspto-grants-1980_07 |