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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037808Generated: October 26, 2026

Hydrochloric Acid → N-(2,6-Dichlorobenzoyl)-4-nitro-L-phenylalanine

https://huagongshe.com/reaction/1037808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Nitro-3-phenyl-L-alanineHCID 13706—
ReactantSodium HydroxideHCID 14798—
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductN-(2,6-Dichlorobenzoyl)-4-nitro-L-phenylalanineHCID 5801832295%

Reaction Steps

To 13 mL of acetone, there were added 10.04 g of p-nitro-L-phenylalanine and 28 mL of water to thus form a suspension and the latter was cooled in an ice-bath. To this suspension, there were alternatively dropwise added 18.4 mL of a 6M sodium hydroxide solution and 10.05 g of 2,6-dichlorobenzoyl chloride in such a manner that the pH value of the suspension was maintained at a level of not less than 13 at a temperature of not more than 15° C. After the completion of the dropwise addition, the suspension was further stirred for 2 hours with cooling in an ice-bath, then the progress of the reaction was confirmed by HPLC and 36 mL of a 2M hydrochloric acid solution was dropwise added while taking care to prevent any excess generation of heat. The suspension containing separated solid matter was stirred at 10° C. overnight, the precipitates were isolated through filtration and then dried under reduced pressure at 60° C. to thus obtain 17.32 g of the title compound as a white crystalline solid (yield: 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546610B2
Source datasetuspto-grants-2013_10
ORD IDord-1b4bdba8796c405cab232e9256ed366e
Source noteuspto-grants-2013_10