Triethylamine → 1175-97-9

HRID 1606432Notes

Reaction equation

HRID 1606432 reaction equation
[CH3:1][C:2]1([CH3:24])[S:6][C@@H:5]2[C@H:7]([NH:10][C:11]([C@H:13]([NH2:20])[C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=3)=[O:12])[C:8](=[O:9])[N:4]2[C@H:3]1[C:21]([OH:23])=[O:22].O.O.O.S([O-])([O-])(=O)=O.[Mg+2].[CH2:34]([N:36]([CH2:39][CH3:40])[CH2:37][CH3:38])[CH3:35]>ClCCl>[CH3:1][C:2]1([CH3:24])[S:6][C@@H:5]2[C@H:7]([NH:10][C:11]([C@H:13]([NH2:20])[C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[O:12])[C:8](=[O:9])[N:4]2[C@H:3]1[C:21]([OH:23])=[O:22].[CH2:34]([N:36]([CH2:39][CH3:40])[CH2:37][CH3:38])[CH3:35]

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 23565Ampicillin TrihydrateHCID 24083Sulfuric acid magnesium salt (1:1)

Product 1

HCID 129189941175-97-9

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

After stirring a mixture of 12 g. of ampicillin trihydrate, 9 g. of anhydrous magnesium sulfate, 8.4 ml. of triethylamine, and 190 ml. of dichloromethane for 1 hour at room temperature, the magnesium sulfate was filtered away to provide dichloromethane solution of ampicillin triethylamine salt.

Workup

  1. additiona mixture of 12 g
  2. filtrationthe magnesium sulfate was filtered away

Sources & evidence

ORD record
ord-89d47fffae0c431894d00844f5c02508
Source dataset
uspto-grants-1976_04
Patent number
US03953428

Reaction notes

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