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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838628Generated: November 2, 2026

Malonic Acid → 3-Amino-3-(pyridin-3-yl)propanoic acid

https://huagongshe.com/reaction/1838628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalonic AcidHCID 867—
ReactantMethanolHCID 887—
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantAmmonium AcetateHCID 517165—
SolventEthanolHCID 702—
Product3-Amino-3-(pyridin-3-yl)propanoic acidHCID 360654749.3%

Reaction Conditions

Temperature78 °C

Reaction Steps

Ammonium acetate (194.28 g, 2.52 mol) was suspended in ethanol (285 g). A solution of pyridine-3-carbaldehyde (62.9 g, 1.68 mol) in ethanol (80 g) was added to the suspension within 10 min at 15° C.-20° C. The reaction mixture was stirred for 1 h until a clear yellowish solution was formed. A suspension of malonic acid (174.86 g, 1.68 mol) in ethanol (235 g) was then added (within 30 min.) After stirring for 30 min at ambient temperature the reaction mixture was heated for 5 h to reflux (78° C.). Gas evolution was observed. After 3-4 h a white solid started to precipitate. The orange colored suspension was cooled to 15° C.-20° C., and a thick slurry was obtained. To this slurry was added methanol (80 g) and the reaction mixture was again heated to reflux (65° C.). The suspension was filtered hot, and the filtercake was washed with three portions of hot methanol (120 g) (at a temperature of 55° C.-65° C.). The wet product was dried in vacuo at 70° C.-80° C. to yield the product as a colorless solid (137.73 g, 49.3%). LC purity 95.8%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673926B2
Source datasetuspto-grants-2004_01
ORD IDord-9f10d55ac1954e2391fb555b238fb673
Source noteuspto-grants-2004_01