HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

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

HRID 1702063
Notes
Print preview

Reaction equation

HRID 1702063 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
ParticipantsProcedureWorkupSources & evidenceReaction notes

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 962
Water
Solvent

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-89d2105cd5bb4937a388b06b312a2782
Source dataset
uspto-grants-1983_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04379922

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes