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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243977Generated: October 30, 2026

Pinacolone → 4-Chlorobenzoic Acid

https://huagongshe.com/reaction/1243977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPinacoloneHCID 6416—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium HydroxideHCID 14798—
CatalystTributylmethylammonium chlorideHCID 91822—
SolventWaterHCID 962—
Product4-Chlorobenzoic AcidHCID 6318—
Product4-ChlorobenzaldehydeHCID 7726—

Reaction Conditions

Temperature40 °C

Reaction Steps

In a 100 gallon stainless steel reactor was charged pinacolone (154.5 kg, 94% pure, 1453 moles), methyltributylammonium chloride (1.09 kg, 75% aqueous solution, 3.47 moles) and water (2.23 kg) and the reactor contents were heated to 40° C. Melted p-chlorobenzaldehyde (109.1 kg, 97.5% pure, 757.1 moles) addition was then started at a rate of 1.82 kg/min (the complete addition therefore took 60 minutes). Ten minutes after the start of the addition of the aldehyde, NaOH (12.36 kg, 50 wt % aqueous solution, 154.5 moles) addition was started at a rate of 0.41 kg/min (the complete addition therefore took 30 minutes). After the addition of the aldehyde was complete, the reactor temperature was increased to 60° C. and heated at that temperature for 3 hours. At that point analysis of the reaction mixture by LC (after negecting the pinacolone and a small amount of p-chlorobenzoic acid formed by air oxidation of the p-chlorobenzaldehyde) indicated that the organic phase contained 96.3% Phenyl aldol and 0.3% unreacted p-chlorobenzaldehyde. The reaction mixture was neutralized with 36% aqueous hydrochloric acid till pH 8.0 and the phases were allowed to settle. The aqueous (lower) phase was discarded and the organic phase was subjected to distillation under reduced pressure to recover all the excess pinacolone. The residue (166.1 kg) was the product Phenyl aldol and was found to be 96.8% pure which translates to a yield of 95.4% based on p-chlorobenzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119234B2
Source datasetuspto-grants-2006_10
ORD IDord-70d67e190bc6427483e7e4d4abf15e5b
Source noteuspto-grants-2006_10