HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1-(Bromomethyl)-4-chloro-2-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | 4-Chloro-2-nitrobenzyl alcohol | HCID 89956 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(Bromomethyl)-4-chloro-2-nitrobenzene | HCID 10586816 | — |
Reaction Steps
To a stirred solution of 10 g of 4-chloro-2-nitrobenzyl alcohol in 200 mL of ether is added dropwise a solution of 17.7 g phosphorus tribromide in 100 mL of ether. The temperature of the reaction mixture is maintained at 15° or lower by means of cooling with an ice-water bath. On completion of the addition the reaction mixture is allowed to stir for an additional 1 hour at 15° and then at room temperature overnight. The reaction mixture is neutralized with 100 mL of 3N sodium hydroxide, and the layers are separated. The ethereal extracts are washed with 2×250 mL of brine, dried over anydrous sodium sulfate; the solvent is evaporated to dryness under reduced pressure to yield 4-chloro-2-nitrobenzyl bromide melting at 50°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04596799 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-8408fcf497ee45739ca636d2887ed467 |
| Source note | uspto-grants-1986_06 |