HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 1-(Bromomethyl)-4-ethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Ethylbenzyl alcohol | HCID 13034 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(Bromomethyl)-4-ethylbenzene | HCID 12231560 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
35 ml of a 33% solution of HBr in AcOH are cooled to 0° C., 5 g of 4-ethylbenzyl alcohol are added dropwise and the reaction mixture is stirred for 30 minutes at 0° C. and then overnight at RT. It is poured into 200 ml of iced water, the mixture is extracted with AcOEt, the organic phase is washed with saturated aqueous NaHCO3 solution and with saturated NaCl solution, dried over Na2SO4 and the solvent is evaporated off under vacuum to give 5.6 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-5df20a6eb1134741993eba5d0b72ce36 |
| Source note | uspto-grants-1999_07 |