Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579372Generated: November 1, 2026

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

https://huagongshe.com/reaction/1579372

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-12N 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 numberUS03931195
Source datasetuspto-grants-1976_01
ORD IDord-b68d55a12b914ae396335f39f68b8d1a
Source noteuspto-grants-1976_01