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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443335Generated: October 29, 2026

Benzaldehyde → α-Phenyl-2-pyridineethanol

https://huagongshe.com/reaction/443335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
Reactant2-MethylpyridineHCID 7975—
ReactantHCID 178506676HCID 178506676—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Productα-Phenyl-2-pyridineethanolHCID 95435—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4.65 grams (0.05 mole) of 2-picoline in 40 milliliters of ether was added, with stirring, to a solution of phenyllithium (0.05 mole) in 30 milliliters of benzene diluted with 50 milliliters of ether. The solution was refluxed for 1 hour and then cooled to 0° C.; a solution of 5.3 grams (0.05 mole) of benzaldehyde in 30 milliliters of ether was added slowly at 0° C. The reaction mixture was stirred at room temperature for 30 minutes. Water was added, and the organic layer was separated and washed with water. Methylene chloride (100 milliliters) was added; the solution was dried over magnesium sulfate and evaporated under reduced pressure to give a solid. The solid was stirred with 50 milliliters of ether, filtered, and washed with 20 milliliters of ether to give 4.1 grams (40%) of virtually pure product. Recrystallization from 1:1 hexane-acetone gave plates, m.p. 105°-107° C. (Lit. m.p., 110° C., Beyerman, H. C., W. Eveleens, and Y. M. F. Muller, Rec. Trav. Chim., 75, 1956, p. 63).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259969
Source datasetuspto-grants-1981_04
ORD IDord-02d3a4c6c04a40dea94ec1dbf6d2b68e
Source noteuspto-grants-1981_04