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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331259Generated: October 30, 2026

Benzaldehyde → T5637827

https://huagongshe.com/reaction/331259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant3-HydroxyacetophenoneHCID 8487—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
ProductT5637827HCID 535638298%

Reaction Conditions

Temperature10 °C

Reaction Steps

A 250 mL round-bottomed flask was charged sequentially aq. NaOH solution (NaOH 7.1 g/H2O 50 mL) and EtOH (40 mL). The solution was maintained below 10° C. in an ice bath. 1-(3-hydroxyphenyl)ethanone (20.0 g, 147 mmol) was added and stirred for 30 min at 10° C. To the resulting mixture was then added benzaldehyde (15 mL, 1.0 eq). After being stirred for additional 1 h at 10° C., the reaction mixture was stirred at room temperature for further 26 h. The solution was concentrated by rotary evaporation under reduced pressure. The residue was dissolved in EtOAc. The organic layer was washed with 3N HCl and H2O, dried over MgSO4, and concentrated in vacuo to obtain the desired product (32.5 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877747B2
Source datasetuspto-grants-2014_11
ORD IDord-b29e8f2f974d49dc81c4aea49cd65a8c
Source noteuspto-grants-2014_11