HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Iodonaphthalene → 5-(1-Naphthyl)-4-pentyn-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Iodonaphthalene | HCID 7004 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Pentyn-1-ol | HCID 79346 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(1-Naphthyl)-4-pentyn-1-ol | HCID 19955557 | 82.9% |
Reaction Steps
A solution of 0.59 g (7 mmol) of 4-pentyn-1-ol in 3 ml of acetonitrile is added dropwise under an argon atmosphere to a suspension of 1.78 g (7 mmol) of 1-iodonaphthalene, of 1.48 ml (10.5 mmol) of triethylamine, of 0.066 g (0.35 mmol) of cuprous iodide and of 0.147 g (0.21 mmol) of di(triphenylphosphine)palladium dichloride (Ph3P)2PdCl2 in 4 ml of acetonitrile. The mixture is stirred at ambient temperature for 3 hours, 4 g of silica are then added and the mixture is evaporated to dryness. The product is purified by chromatography on silica gel, elution being carried out with an 80/20 and then 60/40 mixture of cyclohexane and of ethyl acetate, to produce 1.22 g of product in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645757B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-0e24158261e141b191a3dcee34a14136 |
| Source note | uspto-grants-2010_01 |