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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839256Generated: October 31, 2026

Trichloroacetic Acid → 2-(carbamoylamino)-2-phenylacetic acid

https://huagongshe.com/reaction/839256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetic AcidHCID 6421—
Reactant4-(Dimethylamino)BenzaldehydeHCID 7479—
ReactantSodium CarbonateHCID 10340—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131711120HCID 131711120—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product2-(carbamoylamino)-2-phenylacetic acidHCID 4525385—

Reaction Steps

Mixtures of (1) 2.0 ml. of an aqueous substrate suspension prepared by suspending DL-5-phenylhydantoin into a 0.1 M NaHCO3 --Na2CO3 buffer solution of pH 9.5 (substrate concentration: 1.0%) and (2) 2.0 ml. of the above cell suspension were prepared and placed in test tubes, respectively. The hydrolysis reaction was then carried out at 37° C. for 1 hour with mild shaking. Immediately after the completion of the reaction, 1.0 ml. of a 10% aqueous solution of trichloroacetic acid, 1.0 ml. of a 10% solution of p-dimethylaminobenzaldehyde in 6 N hydrochloric acid and 6.0 ml. of distilled water were added to each reaction mixture and admixed. The resulting each color-developed reaction mixture was centrifuged to remove insoluble materials, and the amounts of N-carbamoyl-2-phenylglycine produced in the reaction mixtures were colorimetrically determined by measuring the absorbance at 420 nm. As a Control, the above procedures were repeated except that no hydantoin compound was employed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04094741
Source datasetuspto-grants-1978_06
ORD IDord-7f4c418ac0e24c6da0ab97e58fa50c9b
Source noteuspto-grants-1978_06