HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-(1-Bromovinyl)-3-chlorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzene, 1-chloro-3-(1,2-dibromoethyl)- | HCID 10870257 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(1-Bromovinyl)-3-chlorobenzene | HCID 11063887 | 99% |
Reaction Steps
In 50 ml of ethanol was suspended 20.8 g (69.7 mmol) of 3-chloro-α,β-dibromoethylbenzene. To the suspension was added 100 ml of an ethanol solution containing 5.8 g (103.4 mmol) of potassium hydroxide at room temperature, and the mixture was stirred at room temperature for 1 hour. After completion of the reaction, the reaction mixture was poured into 150 ml of ice-water and extracted with 300 ml of diethyl ether. The extract was dried over anhydrous sodium sulfate and concentrated to give 15.0 g (purity: 99%) of 3-chloro-α-bromostyrene. 1H-NMR (CDC13, 8): 5.82 (1H, d), 6.14 (1H, d), 7.26-7.33 (2H, m), 7.45-7.49 (1H, m), 7.57-7.58 (1H, m)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05841004 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-99ca9ae8663040e6a01e6cd801436cbc |
| Source note | uspto-grants-1998_11 |