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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404649Generated: November 1, 2026

4-Hydroxybenzaldehyde → HCID 86645079, compound

https://huagongshe.com/reaction/1404649

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 vacuo 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 numberUS08912335B2
Source datasetuspto-grants-2014_12
ORD IDord-40d547a89a0c476ca1e32eab8c572631
Source noteuspto-grants-2014_12