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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1096191Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-(3,4-Dichloro-phenylamino)-propionic Acid

https://huagongshe.com/reaction/1096191

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktL-AlanineHCID 5950—
EduktPotassium Phosphate, TribasicHCID 62657—
EduktBenzene, 1,2-dichloro-4-iodo-HCID 88591—
Edukt2-Hydroxybenzaldehyde phenylhydrazoneHCID 249842—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(3,4-Dichloro-phenylamino)-propionic AcidHCID 691642683,9%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 3,4-dichloroiodobenzene (1.50 g, 5.50 mmol), L-alanine (734 mg, 8.25 mmol), copper(I) iodide, 2-hydroxybenzaldehyde phenylhydrazone (233 mg, 1.10 mmol), tri-potassium phosphate (3.50 g, 16.5 mmol), and N,N-dimethylformamide (8 mL) was stirred at 80° C. for 40 h, then after cooling diluted with water and acidified to pH 3 by addition of 37% aq. HCl solution. The mixture was extracted with EtOAc, the organic phase was washed with brine, dried (MgSO4), filtered, and evaporated. Chromatography (SiO2; EtOAc) afforded the title compound (1.08 g, 67%) as a 71:29 mixture of the (S) and (R) stereoisomers (accordingly, when D-alanine was used instead of L-alanine as starting material, the title compound was obtained as a 29:71 mixture of the (S) and (R) stereoisomers). Brown solid, MS: 232.1 (M−H)−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08138175B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-ba18df7b02184cea8a743c632e8b5caf
Quellennotizuspto-grants-2012_03