HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (4-Iodo-but-2-ynyloxy)-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (4-Hydroxy-but-2-ynyloxy)-acetonitrile | HCID 86012515 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Iodo-but-2-ynyloxy)-acetonitrile | HCID 86012516 | 92% |
Reaction Steps
Triphenylphosphine (10.94 g, 41.7 mmol) and iodine (10.55 g, 41.6 mmol were added sequentially to a solution of (4-hydroxy-but-2-ynyloxy)-acetonitrile (4.35 g, 34.8 mmol) in CH2Cl2 (100 mL). The reaction mixture became homogeneous after 5 min at rt and imidazole (2.76 g, 40.5 mmol) was added slowly in small portions. After 1.5 h at rt, the reaction was filtered through activity I basic alumina, washing with 20% EtOAc/Hexane. The filtrate was concentrated in vacuo then purified by flash column chromatography on silica gel (hexane→10% EtOAc/hexane, gradient) to afford 7.51 g (92%) of (4-iodo-but-2-ynyloxy)-acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179820B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-9b79928d940f40fb95dddc7f4bb9f9ef |
| Source note | uspto-grants-2007_02 |