HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 1-(1-Bromoethyl)-2,4-dichlorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(2,4-Dichlorophenyl)ethan-1-ol | HCID 92889 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(1-Bromoethyl)-2,4-dichlorobenzene | HCID 43141435 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
15 ml of a 33% solution of HBr in AcOH are cooled to 0° C., 2 ml of 2,4-dichloro-1-(1-hydroxyethyl)benzene are added dropwise and the reaction mixture is stirred for 30 minutes at 0° C. and then for 3 hours at RT. It is poured into iced water and extracted with AcOEt, the organic phase is washed with saturated aqueous NaHCO3 solution, with water and with saturated NaCl solution and dried over MgSO4 and the solvent is evaporated off under vacuum to give 3.4 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05925768 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-282ddd08c7094b82a49b2af700d2225f |
| Source note | uspto-grants-1999_07 |