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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096191Generated: October 25, 2026

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

https://huagongshe.com/reaction/1096191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantL-AlanineHCID 5950—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantBenzene, 1,2-dichloro-4-iodo-HCID 88591—
Reactant2-Hydroxybenzaldehyde phenylhydrazoneHCID 249842—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(3,4-Dichloro-phenylamino)-propionic AcidHCID 691642683.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

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)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138175B2
Source datasetuspto-grants-2012_03
ORD IDord-ba18df7b02184cea8a743c632e8b5caf
Source noteuspto-grants-2012_03