Ethylenediamine → HCID 86739113, compound

HRID 1649491Notes

Reaction equation

HRID 1649491 reaction equation
O.C1(C)C=CC(S(O)(=O)=O)=CC=1.[C:13]12[C:26](=[O:27])[O:25][C:23](=O)[C:14]=1[CH2:15][CH2:16][C:17]1[C:22]2=[CH:21][CH:20]=[CH:19][CH:18]=1.[CH2:28]([NH2:31])[CH2:29][NH2:30]>C1(C)C=CC=CC=1>[NH2:30][CH2:29][CH2:28][N:31]1[C:23](=[O:25])[C:14]2[CH2:15][CH2:16][C:17]3[C:22]([C:13]=2[C:26]1=[O:27])=[CH:21][CH:20]=[CH:19][CH:18]=3

Participants

5

Reactant 3

HCID 3301EthylenediamineHCID 1422143,4-Dihydro-1,2-naphthalenedicarboxylic anhydrideHCID 521998p-Toluenesulfonic acid monohydrate

Product 1

HCID 86739113HCID 86739113, compoundYield 97.8%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Conditions

Temperature
60 °C

Procedure

27.6 g of toluene-p-sulphonic acid monohydrate are added to a solution of 27.62 g (0.138 mol) of 3,4-dihydronaphthalene-1,2-dicarboxylic acid anhydride in 300 ml of toluene, followed by 8.69 g of ethylenediamine. The mixture is heated to 60° C. for 30 minutes and then refluxed for 30 minutes, removing continuously the toluene and the water as they are formed by destillation. The residue is dried under vacuo to yield 32.7 g (90.0% of theory) of N-(2'-aminoethyl)-3,4-dihydronaphthalene-1,2-dicarboximide in the form of its toluene-p-sulphonic acid salt. This salt may be purified by recrystallisation from toluene.

Workup

  1. temperaturerefluxed for 30 minutes
  2. customremoving continuously the toluene
  3. customthe water as they are formed by destillation
  4. customThe residue is dried under vacuo

Sources & evidence

ORD record
ord-146e70530f004110832be50d83449d2e
Source dataset
uspto-grants-1983_11
Patent number
US04417058

Reaction notes

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