HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 3,7,11-Trimethyl-1-dodecyl iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3,7,11-Trimethyl-1-dodecanol | HCID 138824 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3,7,11-Trimethyl-1-dodecyl iodide | HCID 57887311 | 61% |
Reaction Steps
To a stirring solution of 44 (1.5 g, 6.6 mmol), imidazole (1.13 g, 16.6 mmol, 2.5 equ) and triphenylphosphine (4.40 g, 16.8 mmol, 2.5 equ) in toluene (250 ml) under nitrogen was added iodine (3.26 g, 12.8 mmol, 1.9 equ). The reaction mixture was stirred for one hour then filtered. The filtrate was washed with 8% sodium thiosulphate solution (250 ml) and brine (100 ml) then dried (Na2SO4) and concentrated in vacuo to give a white solid. This solid was taken up in hexane, cooled and filtered. The filtrate was then concentrated in vacuo to give 46 (1.1 g, 61%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601754B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-fc4cd3b027a04ea39799505ca8f5eb8d |
| Source note | uspto-grants-2009_10 |