HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-Chloro-3-Methoxy-2-(Cyclopropyl)-Methyl Pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Bromocyclopropane | HCID 78037 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 18675872 | HCID 18675872 | — |
| Product | 4-Chloro-3-Methoxy-2-(Cyclopropyl)-Methyl Pyridine | HCID 18675868 | — |
Reaction Conditions
| Temperature | -45 °C |
|---|
Reaction Steps
Cyclopropyl bromide (0.5 ml) is dissolved in 5 mnl of THF and magnesium (0.15 g) is added and heat is applied to initiate the reaction. Once the reaction is completed, the solution is cooled to −45° C. and cuprous iodide (0.5 g) is added. The reaction is allowed to stir for 30 minutes and 4-Chloro-3-methoxy-2-bromomethyl-pyridine (0.154 g) is added. The reaction is stirred at −45° C. for one hour and allowed to warm at room temperature before being quenched by 5 ml of 28% ammonium hydroxide. The reaction is extracted with ether and the desired product purified by chromatography using hexane/ethyl acetate 9/1 as solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06509349B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-615e67ab95604eecb7eca7fe4ac70e56 |
| Source note | uspto-grants-2003_01 |