HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 2-benzyloxy-5-nitro-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-benzyloxy-5-nitro-pyridine | HCID 295676 | — |
Reaction Steps
32 g (0.20 mol) 2-chloro-5-nitropyridine in 120 mL toluene were combined with 200 mL (0.20 mmol) of a 1M sodium benzylate solution in benzylalcohol and stirred overnight at RT. The organic phase was washed with water and saturated sodium chloride solution, dried on sodium sulphate and the toluene was eliminated by distillation. The residue was cooled with ice, the precipitate formed was suction filtered and washed several times with tert.-butylmethylether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829006B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-d214f498422c427f90ac0c65a1d705e9 |
| Source note | uspto-grants-2014_09 |