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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichloroacetic Acid | HCID 6421 | — |
| Reactant | 4-(Dimethylamino)Benzaldehyde | HCID 7479 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 131711120 | HCID 131711120 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(carbamoylamino)-2-phenylacetic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04094741 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-7f4c418ac0e24c6da0ab97e58fa50c9b |
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| Source note | uspto-grants-1978_06 |
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