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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585089Generated: October 30, 2026

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

https://huagongshe.com/reaction/585089

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 numberUS06930112B2
Source datasetuspto-grants-2005_08
ORD IDord-5015f08117b345f8a15c6f310c74c613
Source noteuspto-grants-2005_08