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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916174Generated: October 30, 2026

Malonic Acid → (RS)-beta-Amino-beta-(4-bromophenyl)propionic acid

https://huagongshe.com/reaction/916174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalonic AcidHCID 867—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantAmmonium AcetateHCID 517165—
SolventEthanolHCID 702—
Product(RS)-beta-Amino-beta-(4-bromophenyl)propionic acidHCID 55403434.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

4-Bromobenzaldehyde (10 g, 54 mmol), ammonium acetate (8.663 g, 112.4 mmol) and malonic acid (5.6762 g, 54.5 mmol) were refluxed (slow) in absolute ethanol (45 mL) for 150 hours. White solid was filtered and dissolved into a warm (70° C.) solution of 50 mL of Na2CO3 and 50 mL of H2O. This solution was then extracted with 100 mL of diethyl ether three times. The aqueous layer was further acidified to pH 7 to produce white solid β-4-bromophenyl-β-alanine (4.5140 g, 18.49 mmol, 34.2%); MP: 234° C.; IR (KBr): 3061, 1594 cm−1; TLC: RF=0.35 (solvent 24), 0.32 (solvent 25); 1H NMR (D2O/K2CO3): δ 7.42-7.38 (m, 2H), 7.17-7.14 (m, 2H), 4.11-4.07 (t, J=7.25 Hz, 1H), 2.48-2.36 (m, 2H). Anal. Calcd for C9H10BrNO2: C, 44.29; H, 4.13; N, 5.74. Found: C, 44.35; H, 3.93; N, 5.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268164B2
Source datasetuspto-grants-2007_09
ORD IDord-47878775ca3d45daa129ea7bfe917422
Source noteuspto-grants-2007_09