HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (2-Iodoethyl)cyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Cyclohexylethanol | HCID 20508 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Iodoethyl)cyclohexane | HCID 12923931 | 79% |
Reaction Steps
Into a 250-mL 3-necked round-bottom flask was placed 2-cyclohexylethan-1-ol (3 g, 23.40 mmol, 1.00 equiv), imidazole (2 g, 29.41 mmol, 1.26 equiv), PPh3 (8 g, 30.50 mmol, 1.30 equiv), tetrahydrofuran (60 mL) and I2 (7.7 g, 30.31 mmol, 1.30 equiv). The resulting solution was stirred for 4 h at room temperature. The reaction was then quenched by the addition of 100 mL of sodium bicarbonate (sat.). The resulting solution was extracted with 2×100 mL of ethyl acetate and the organic layers combined and concentrated under vacuum. The residue was applied onto a silica gel column with petroleum ether. Purification afforded 4.4 g (79%) of (2-iodoethyl)cyclohexane as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969557B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-3c76c23b5a6e4de5bc93c1a98a6e1ddb |
| Source note | uspto-grants-2015_03 |