HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 86584312, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3-Pyridinemethanol | HCID 7510 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86584312 | HCID 86584312 | — |
Reaction Steps
To a solution of 3-pyridyl carbinol (100 mmol) in 30 mL of ethanol is added benzyl bromide (110 mmol) dropwise via addition funnel at room temperature. Stirring is continued for 2 hours at room temperature and solvents are removed in vacuo. The residue is taken up into acetonitrile (100 mL) and washed with hexanes (3×100 mL). The acetonitrile layer is concentrated in vacuo and dried under vacuum to provide N-benzyl-3-pyridyl carbinol bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06277865B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-debc630d7a834f53b72f7d4b5c9a69c8 |
| Source note | uspto-grants-2001_08 |