HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 5-(Benzyloxy)-2-(chloromethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (5-(Benzyloxy)pyridin-2-yl)methanol | HCID 11736050 | — |
| Product | 5-(Benzyloxy)-2-(chloromethyl)pyridine | HCID 17854158 | — |
Reaction Steps
To a solution of carbon tetrachloride (10 mL) of a known compound (5-benzyloxy-pyridin-2-yl)-methanol (500 mg) was added triphenylphosphine (791 mg) at room temperature, which was heated to reflux for 19 hours and 35 minutes under a nitrogen atmosphere. The reaction mixture was cooled to room temperature, after which the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=3:1) to obtain the titled compound (386 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183264B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-184e7f8305af4f6ba5128d3214c7811b |
| Source note | uspto-grants-2012_05 |