HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5,5-Trimethyl-1-hexanol → 8-Ethyl-2,2,4-trimethyl-6-dodecanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5,5-Trimethyl-1-hexanol | HCID 18938 | — |
| Reactant | 2-Ethylhexyl bromide | HCID 86804 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | Carbonochloridate | HCID 21226386 | — |
| Reactant | 1-[8-Ethyl-2,2,4-trimethyl-6-dodecyloxycarbonyl]-1,2,4-triazole | HCID 54163492 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Ethyl-2,2,4-trimethyl-6-dodecanol | HCID 19788763 | — |
Reaction Steps
8-Ethyl-2,2,4-trimethyl-6-dodecanol (b.p. 86°-90° at 0.15 mm of mercury pressure) was prepared by reacting 1-bromo-2-ethylhexane and 3,5,5-trimethylhexanol with lithium in tetrahydrofuran at 0° to -10° according to the general method of Pearce, Richards and Scilly (J.Chem. Soc., Perkin I, 1655, 1972). This compound was converted, by way of the chloroformate, into 1-[8-ethyl-2,2,4-trimethyl-6-dodecyloxycarbonyl]-1,2,4-triazole of formula: ##STR18## The compound was evaluated as an extractant for copper by the procedure of Example 1 and the results are presented in Table 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04879388 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-787e0c45442d48f1b5a4d396b2d85c60 |
| Source note | uspto-grants-1989_11 |