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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274346Generated: October 30, 2026

4-Hydroxybenzaldehyde → HCID 86645079, compound

https://huagongshe.com/reaction/2274346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantSodium HydroxideHCID 14798—
Reactant2-(3-Chlorophenyl)oxiraneHCID 155613—
SolventTolueneHCID 1140—
ProductHCID 86645079HCID 8664507910%

Reaction Conditions

Temperature78 °C

Reaction Steps

To a stirring solution of 2-(3-chlorophenyl)oxirane (6.20 g, 40.0 mmol) in toluene (65 mL) was added 4-hydroxybenzaldehyde (7.30 g, 60.0 mmol), 1M NaOH (65 mL) and PEG4000 (polyethylene glycol, 0.85 g) and the stirring mixture was heated at 78° C. for three hours. The reaction was allowed to cool to RT and then extracted with EtOAc (2×150 mL). The combined extracts were washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The resulting light brown oil was adsorbed onto silica gel and chromatographed eluting with 25-40% EtOAc/hexanes. There are 2 major spots. Fractions containing the higher Rf spot were combined and evaporated in vacuo to give 1.08 g (10%) of the desired product as a colorless oil. Fractions containing the lower Rf spot were combined and evaporated in vauo to give 0.95 g (8%) of the regioisomer as a colorless oil, 44B. Some starting epoxide (2.85 g) was also recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126959B2
Source datasetuspto-grants-2015_09
ORD IDord-0681bbc3b5c5485888b814f8746367b9
Source noteuspto-grants-2015_09