Hydrochloric Acid → 7-Amino-3-methylenecepham-4-carboxylic acid

HRID 1154819Notes

Reaction equation

HRID 1154819 reaction equation
CC(O[CH2:5][C:6]1[CH2:15][S:14][C@@H:9]2[C@H:10]([NH2:13])[C:11](=[O:12])[N:8]2[C:7]=1[C:16]([OH:18])=[O:17])=O.Cl.[OH-].[Na+]>O.[Zn]>[NH2:13][CH:10]1[C:11](=[O:12])[N:8]2[CH:7]([C:16]([OH:18])=[O:17])[C:6](=[CH2:5])[CH2:15][S:14][C@H:9]12

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 4413287-Aminocephalosporanic acid

Product 1

HCID 130225477-Amino-3-methylenecepham-4-carboxylic acidYield 55.7%

Reagents, catalysts & solvents 2

HCID 23994ZincCatalystHCID 962WaterSolvent

Procedure

Zinc powder (40 g) was added to a solution of 7-aminocephalosporanic acid (27.3 g) and conc. hydrochloric acid (70 ml.) in water (200 ml.) for 5° C. and stirred for an hour. The resultant solution was adjusted to pH 4.0 with 4 N sodium hydroxide and concentrated to 100 ml. of the volume. After adjusting the solution to pH 4.0, the solution was allowed to stand under cooling overnight. The precipitates were collected by filtration to give 7-amino-3-methylenecepham-4-carboxylic acid (11.96 g.).

Workup

  1. concentrationconcentrated to 100 ml
  2. temperatureunder cooling overnight
  3. filtrationThe precipitates were collected by filtration

Sources & evidence

ORD record
ord-d24ac584d86e472ebaf35bbb4ce2f5ee
Source dataset
uspto-grants-1981_11
Patent number
US04298529

Reaction notes

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