HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → Phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Nickel monomethoxide | HCID 22477019 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Phenol | HCID 996 | — |
| Product | Nickel monomethoxide | HCID 22477019 | — |
Reaction Steps
[2,2'-thiobis-(4-t-octyl-phenolato)]-benzyl alcohol Nickel II, NiTBP.C6H5OH was prepared as follows: p [2,2'-thiobis-(4-t-octylphenolato)]-2-propanol nickel II prepared as described in Example 4 (83.9 g) was dissolved in benzene (250 ml) and benzyl alcohol (16.2 g) was then added. The resulting solution was heated and refluxed for 1 hr. The displaced 2-propanol and most of the benzene solvent was then removed by distillation and the remainder by rotary evaporation. The complex[2,2'-thiobis-(4-t-octylphenolato)]benzyl alcohol nickel II was thus obtained as a green solid which softened at 150° C., melted partially at 210° C. and was completely fused at 260° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04198303 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-b58532c9e4624da39029dc8838fa7f8d |
| Source note | uspto-grants-1980_04 |