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

HRID 839256Notes

Reaction equation

HRID 839256 reaction equation
COC1C=C(CNCCCNCCCCNCCCN)C=CC=1O.C1([N:31]2CC(=O)[NH:34][C:32]2=[O:33])C=CC=CC=1.[C:38]([O-:41])(O)=[O:39].[Na+].C([O-])([O-])=O.[Na+].[Na+].ClC(Cl)(Cl)C(O)=O.CN(C)[C:58]1[CH:65]=[CH:64][C:61]([CH:62]=O)=[CH:60][CH:59]=1>Cl.O>[C:32]([NH:34][CH:62]([C:61]1[CH:60]=[CH:59][CH:58]=[CH:65][CH:64]=1)[C:38]([OH:41])=[O:39])(=[O:33])[NH2:31]

Participants

8

Procedure

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.

Workup

  1. customof an aqueous substrate suspension prepared
  2. customof the above cell suspension were prepared
  3. customThe hydrolysis reaction
  4. customImmediately after the completion of the reaction, 1.0 ml
  5. customto remove insoluble materials

Sources & evidence

ORD record
ord-7f4c418ac0e24c6da0ab97e58fa50c9b
Source dataset
uspto-grants-1978_06
Patent number
US04094741

Reaction notes

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