HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 2-Bromo-1-(3-chlorophenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Benzene, 1-chloro-3-(1,2-dibromoethyl)- | HCID 10870257 | — |
| Product | 2-Bromo-1-(3-chlorophenyl)ethanol | HCID 9964694 | — |
Reaction Steps
To 996 g of 3-chloro-α,β-dibromoethylbenzene were added 10.8 g of potassium iodide and 3.5 l of water. The mixture was then heated under reflux for 49 hours while the released free iodine was being removed. After the termination of the reaction, the reaction solution was allowed to cool to room temperature. The oil phase separated was separated and then washed with water for neutralization to give 714 g of 2-bromo-1-(3-chlorophenyl)ethanol was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05841001 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-d48780cf21f24d00be53fed2ae04e2dd |
| Source note | uspto-grants-1998_11 |