HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 2-(6-(Bromomethyl)pyridin-2-yl)propan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(6-(Hydroxymethyl)pyridin-2-yl)propan-2-ol | HCID 19104316 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(6-(Bromomethyl)pyridin-2-yl)propan-2-ol | HCID 66718388 | 74.2% |
Reaction Steps
To a solution of 2-hydroxymethyl-6-(1-hydroxy-1-methylethyl)pyridine (5.1 g, 30.5 mmol) in dichloromethane (300 mL) was added carbon tetrabromide (8.81 g, 33.6 mmol) and triphenylphosphine (11.14 g, 33.6 mmol). The reaction was stirred at ambient temperature overnight then poured into a saturated solution of sodium bicarbonate. The organic layer was separated, concentrated to dryness and purified by column chromatography, eluting with a gradient of hexane to 3:1 hexane:ethyl acetate. The title compound (5.21 g, 74%) was obtained as a colourless oil; LC-MS Retention time 2.08 min, (M+H)+ 230, 232
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450328B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-9eb25747eb564f8482917e17d353fb85 |
| Source note | uspto-grants-2013_05 |