HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 1,2-Octanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | 1-Octene | HCID 8125 | — |
| Reactant | Perhydroxyl radical | HCID 18500 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1,2-Octanediol | HCID 14231 | — |
Reaction Steps
Into a 100 ml 3-neck flask provided with condenser, addition funnel, and magnetic stirrer is charged t-butyl-alcohol (20.0 g), 1-octene (4.48 g), water (1.0 g), NaI (0.03 g) and 0.30 g of the Os(CO)12 /MgO supported catalyst prepared in accordance with Example 1. At ambient temperature (26° C.), 2.0 g of a solution of 90% by weight, tertiary butyl hydroperoxide dissolved in t-butyl alcohol is added dropwise over a period of 2 minutes with stirring. After 12 hours from completion of the addition, the reaction mixture is analyzed by GLC and complete conversion of the hydroperoxide is obtained with a selectivity to 1,2-octanediol of 84%. The results are summarized at Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04413151 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-4827ab09b1c74073ab269da1b37c4b92 |
| Source note | uspto-grants-1983_11 |