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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | 2-Methylpyridine | HCID 7975 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(p-Bromophenyl)-1-(2-pyridyl)-2-propanol | HCID 20560115 | 63% |
| Product | 2-[2-(4-Bromophenyl)prop-1-en-1-yl]pyridine | HCID 54180662 | 26% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE030812 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-a9d27b58eac14c00a4e76034f2dc212c |
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| Source note | uspto-grants-1981_12 |
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