Trichloroacetic Acid → 2-(carbamoylamino)-2-phenylacetic acid
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
Reactant 5
Product 1
Reagents, catalysts & solvents 2
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
- customof an aqueous substrate suspension prepared
- customof the above cell suspension were prepared
- customThe hydrolysis reaction
- customImmediately after the completion of the reaction, 1.0 ml
- 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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