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HRID 2095503Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2095503

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium Phosphate, TribasicHCID 62657—
EduktD-AlanineHCID 71080—
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—
Produkt(R)-2-(3,4-Dichloro-phenylamino)-propionic acidHCID 18214660,4%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 6.00 g (22.00 mmol) 3,4-dichloroiodobenzene, 2.94 g (33.00 mmol) D-alanine, 0.42 g (2.20 mmol) copper(I) iodide, 0.96 g (4.40 mmol) 2-hydroxybenzaldehyde phenylhydrazone, 14.00 g (66.00 mmol) tri-potassium phosphate in 32 ml of N,N-dimethylformamide was stirred at 80° C. for 16 h under argon, then after cooling diluted with water and acidified to pH 3 by addition of 25% aq. HCl solution. The mixture was extracted with EtOAc (3×), the organic phases were washed with brine, dried (Na2SO4), filtered and evaporated. Flash chromatography (SiO2; dichloromethane/MeOH 95:5 to 4:1) afforded 3.11 g (60%) of the title compound (as 81:19 mixture of the (R) and (S) stereoisomers, BGB-175*0.25 column) as light brown solid. MS: 231.9 (M−H−, 2Cl).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08445674B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-762c2d4777384a30afd91c16ba20d130
Quellennotizuspto-grants-2013_05