Acetic Acid → HCID 131715137, compound

HRID 653238Notes

Reaction equation

HRID 653238 reaction equation
C([NH:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[CH2:19][C:20]([NH:22][CH:23]1[CH2:26][N:25]([S:27]([O-:30])(=[O:29])=[O:28])[C:24]1=[O:31])=[O:21])(OCC1C=CC=CC=1)=O.[Na+:32].C(O)(=O)C>CO.[H][H].[Pd]>[NH2:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[CH2:19][C:20]([NH:22][CH:23]1[CH2:26][N:25]([S:27]([O-:30])(=[O:28])=[O:29])[C:24]1=[O:31])=[O:21].[Na+:32]

Participants

6

Reactant 2

HCID 176Acetic AcidHCID 23705552HCID 23705552, compound

Product 1

HCID 131715137HCID 131715137, compoundYield 77.9%

Reagents, catalysts & solvents 3

HCID 23938PalladiumCatalystHCID 887MethanolSolventHCID 178418361HCID 178418361, compoundSolvent

Procedure

In 35 ml of 30% methanol is dissolved 0.30 g of the above sodium 3-[2-(2-carbobenzoxyaminomethylphenyl)acetamido]-2-oxoazetidine-1-sulfonate, followed by addition of 0.68 ml of 6% acetic acid and 76 mg of palladium black. The mixture is stirred in hydrogen gas streams at room temperature for 90 minutes. The catalyst is filtered off and the filtrate is purified on an Amberlite XAD-II column. The above procedure provides 0.167 g of sodium 3-[2-(2-aminomethylphenyl)acetamido]-2 -oxoazetidine-1-sulfonate.acetate.

Workup

  1. filtrationThe catalyst is filtered off
  2. customthe filtrate is purified on an Amberlite XAD-II column

Sources & evidence

ORD record
ord-2e40c6ce05b440a49d2150c8c283d557
Source dataset
uspto-grants-1987_06
Patent number
US04675397

Reaction notes

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