HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Benzene, 2-bromo-1,4-dimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | Bromine | HCID 24408 | — |
| Product | Benzene, 2-bromo-1,4-dimethyl- | HCID 11121 | — |
Reaction Steps
This experiment was carried out in two successive steps. In the first stage the total p-xylene was divided into two parts and one-half of the p-xylene was added to the reaction vessel with the catalyst. The other half of the p-xylene and the bromine were then added simultaneously but in separate streams to the flask while maintaining the temperature of the reacting mixture at 20°-25°C. When the reaction was completed as evidenced by no further hydrogen bromide evolution, the resulting mixture was distilled. An initial fraction of monobromo-p-xylene was taken off at 75°-103° (9mm). The 2,5-dibromo-p-xylene was recovered by distillation at 122°-126° (10 mm) as a water-white liquid which solidified to a white, fused, crystalline mass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03932542 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-425a4e8956ee48f5bbb97a9a86633dd6 |
| Source note | uspto-grants-1976_01 |