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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659281Generated: October 31, 2026

Acetic Acid → 2-(p-Bromophenyl)-1-(2-pyridyl)-2-propanol

https://huagongshe.com/reaction/1659281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactantp-BromoacetophenoneHCID 7466—
Reactant2-MethylpyridineHCID 7975—
SolventBenzeneHCID 241—
Product2-(p-Bromophenyl)-1-(2-pyridyl)-2-propanolHCID 2056011563%
Product2-[2-(4-Bromophenyl)prop-1-en-1-yl]pyridineHCID 5418066226%

Reaction Steps

2-(p-Bromophenyl)-1-(2-pyridyl)-2-propanol is prepared from p-bromoacetophenone and 2-picoline according to the method of Villani, et al., J. Med. Chem., 13, 359 (1970) in 63% yield. This alcohol (129.1 g.) is dehydrated by heating in 1150 ml. of acetic acid-12 N hydrochloric acid (3:1) at reflux temperature for 4 hr. The mixture is evaporated in vacuo, made basic with concentrated ammonium hydroxide, and extracted with ethyl acetate. The ethyl acetate extract is washed with water and brine, dried over sodium sulfate, and evaporated to give a dark brown oil. A solution of the oil in benzene is passed through a column of silica gel. Evaporation of the eluate gave 46.4 g (26% yield) of crystalline 2-(p-bromophenyl)-1-(2-pyridyl)propene, m.p. 71.5°-73.5° C. (corr.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE030812
Source datasetuspto-grants-1981_12
ORD IDord-a9d27b58eac14c00a4e76034f2dc212c
Source noteuspto-grants-1981_12