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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613639Generated: October 25, 2026

Ethylene Glycol → 1-(Pyrid-3-yl)-2-(2-bromophenyl)-ethanediol

https://huagongshe.com/reaction/1613639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(Pyrid-3-yl)-2-(2-bromophenyl)-2-hydroxyethanoneHCID 19774196—
SolventMethanolHCID 887—
Product1-(Pyrid-3-yl)-2-(2-bromophenyl)-ethanediolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194441
Source datasetuspto-grants-1993_03
ORD IDord-bcdbc5e5795b45fca221e53df83d02ea
Source noteuspto-grants-1993_03