HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Phenol, 2,2'-[1,2-ethanediylbis(nitrilomethylidyne)]bis[4,6-bis(1,1-dimethylethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | 3,5-Di-tert-butylsalicylaldehyde | HCID 688023 | — |
| Product | Phenol, 2,2'-[1,2-ethanediylbis(nitrilomethylidyne)]bis[4,6-bis(1,1-dimethylethyl)- | HCID 1897040 | — |
Reaction Steps
15 g (0.064 mol) of 3,5-di-tert-butyl salicylaldehyde was dissolved in 500 ml of methanol, and then 1.92 g (0.032 mol) of ethylenediamine was added, and stirred at room temperature for 2 hours. The reaction product thus obtained was filtrated to give 13.3 g (0.0266 mol) of N,N′-bis(3,5-di-tert-butylsalicylidene)ethylenediamine. Next, in a solution obtained by dissolving the above compound in 1000 g of methanol, Co(OAc)2.4H2O was added in an amount of 8.753 g (0.0266 mol), followed by reflux for two hours, and the product thus obtained was subjected to filtration to give a metallosalen complex 1 (N,N′-bis(3,5-di-tert-butylsalicylidene)ethylenediaminato cobalt(II)). The yield was 70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07553243B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-63af253a915541e0b47fa1b39274c3e8 |
| Source note | uspto-grants-2009_06 |