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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013659Generated: November 1, 2026

2-Oxobutanoic Acid → HCID 67017140, compound

https://huagongshe.com/reaction/1013659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Oxobutanoic AcidHCID 58—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(3-Chlorophenyl)ethanoneHCID 14933—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 67017140HCID 67017140—

Reaction Conditions

Temperature0 °C

Reaction Steps

A RBF was charged with 2-oxobutanoic acid (2.50 g, 24.5 mmol) and 3.2 mL of water and the mixture was cooled to 0° C. The acid was neutralized by slow addition of 20% aqueous KOH. 3′-chloroacetophenone (3.79 g, 24.5 mmol) was added, followed by a 1.3 M solution of KOH (2.20 g, 39.2 mmol) in MeOH. The reaction mixture was stirred at 0° C. for 48 h. The mixture was brought to pH 2 by dropwise addition of conc. H2SO4. The MeOH was removed in vacuo, and 25 mL of water was added. The heterogeneous mixture was filtered through Celite, and the filter cake was washed with water and CH2Cl2. The layers of the filtrate were separated, and the aqueous portion was extracted with additional CH2Cl2. The combined organics were dried with MgSO4, filtered and concentrated to a volume of 25 mL. Hexane was added until the mixture became cloudy, and upon standing a white crystalline solid formed. The mother liquor was decanted and the solids were washed with hexane and dried to provide 4-(3-chlorophenyl)-2-ethyl-2-hydroxy-4-oxobutanoic acid as a white crystalline solid. MS m/z=279 [M+Na]+. Calc'd for C12H13ClO4: 256.69.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981891B2
Source datasetuspto-grants-2011_07
ORD IDord-7d461252631847b1b24339249c3b5d30
Source noteuspto-grants-2011_07