HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → 5-(Benzyloxy)-1,3-dimethyl-2-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Dimethyl-4-nitrophenol | HCID 138466 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-(Benzyloxy)-1,3-dimethyl-2-nitrobenzene | HCID 13369956 | 84.5% |
Reaction Steps
A mixture of 3,5-dimethyl-4-nitrophenol (17.6 g), benzyl chloride (20.0 g) and anhydrous K2CO3 (13.2 g) in acetone (100 ml) is stirred under reflux for 22 hours. The reaction mixture is filtered and the precipitate washed with acetone. The acetone extract is concentrated in vacuo and the residue short path distilled (160°-170° C.; 50μ) to give 22.9 grams of an orange liquid which crystallized on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04704401 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-771e103ba1a248bea994b0162b26dd0b |
| Source note | uspto-grants-1987_11 |