HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 1-(Pyrid-3-yl)-2-(2-bromophenyl)-ethanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(Pyrid-3-yl)-2-(2-bromophenyl)-2-hydroxyethanone | HCID 19774196 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(Pyrid-3-yl)-2-(2-bromophenyl)-ethanediol | HCID 19774197 | — |
Reaction Steps
20 g (0.068 mol) of 1-(pyrid-3-yl)-2-(2-bromophenyl)-2-hydroxyethanone in 300 ml of methanol were reduced with 3 g (0.079 mol) of sodium borohydride at 0° C. Stirring was carried out for a few hours at room temperature (21° C.), the pH was brought to 2 with 4N hydrochloric acid and 4 ml of ethylene glycol were added. The solution was evaporated down, after which the residue was covered with a layer of ethyl acetate and neutralized with NaHCO3 solution. The ethyl acetate phase was washed twice with water and dried over Na2SO4. After the ethyl acetate had been distilled off, the product was obtained as a white powder of melting point 115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05194441 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-bcdbc5e5795b45fca221e53df83d02ea |
| Source note | uspto-grants-1993_03 |