HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 5-(Benzyloxy)-2-(bromomethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (5-(Benzyloxy)pyridin-2-yl)methanol | HCID 11736050 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(Benzyloxy)-2-(bromomethyl)pyridine | HCID 79799949 | — |
Reaction Steps
A mixture of 540 mg (2.51 mmol) 5-benzyloxy-2-pyridinemethanol (prepared according to J. Med. Chem. 1977, 20, 1258-1262), 536 mg N-bromo succinimide (3.01 mmol), and 1.2 g polymer bound triphenylphosphine (loading approx. 3 mmol/g, approx. 3.3 mmol) in dichloromethane (40 mL) was stirred overnight at room temperature. All solids were removed by filtration, and the filtrate was washed with aqueous sodium bicarbonate and water, and than concentrated in vacuo. The crude product (540 mg of a slightly pink solid, 79% crude yield) was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238631B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-f5186209fbde4ee48bd077373148255b |
| Source note | uspto-grants-2016_01 |