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HCID 13417979, compound → 2,3-Dihydro-2-(2,2-diethoxyethyl)-3-(1-aminoethyl)-isoindol-1-one

HRID 1680512
Notes
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Reaction equation

HRID 1680512 reaction equation
[CH2:1]([O:3][CH:4]([O:21][CH2:22][CH3:23])[CH2:5][N:6]1[CH:14]([CH:15]([N+:17]([O-])=O)[CH3:16])[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]1=[O:20])[CH3:2]>[Pd].C(O)(=O)C.O>[CH2:22]([O:21][CH:4]([O:3][CH2:1][CH3:2])[CH2:5][N:6]1[CH:14]([CH:15]([NH2:17])[CH3:16])[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]1=[O:20])[CH3:23]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 13417979HCID 13417979, compound

Product 1

HCID 134179842,3-Dihydro-2-(2,2-diethoxyethyl)-3-(1-aminoethyl)-isoindol-1-oneYield 38.8%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 21899381Acetic acid--water (1/1)Solvent

Conditions

Temperature
25 °C

Procedure

A mixture of the two isomers of 2,3-dihydro-2-(2,2-diethoxyethyl)-3-(1-nitroethyl)-isoindol-1-one (2.5 g, described in Example 30) and 10% palladium on carbon (0.25 g) in acetic acid-water (4:1, 50 ml) is stirred under an atmosphere of hydrogen at 50 psi and 25° C. for 18 hr and filtered. The filtrate is evaporated and dissolved in 2% hydrochloric acid. The solution is washed with diethyl ether, basified to pH 9 with ammonium hydroxide and extracted with ethyl acetate. The organic extract is dried, evaporated and chromatographed on silica gel using acetone-benzene (2:3). Evaporation of the eluates gives isomer A (1.14 g) of the title compound, ir (CHCl3) 1675, 1120 and 1050 cm-1 and isomer B (0.88 g) of the title compound, ir (CHCl3) 1675, 1120 and 1050 cm-1.

Workup

  1. filtrationfiltered
  2. customThe filtrate is evaporated
  3. dissolutiondissolved in 2% hydrochloric acid
  4. washThe solution is washed with diethyl ether
  5. extractionextracted with ethyl acetate
  6. extractionThe organic extract
  7. customis dried
  8. customevaporated
  9. customchromatographed on silica gel
  10. customEvaporation of the eluates

Sources & evidence

ORD record
ord-3a905846430242ef88e400831f973ddc
Source dataset
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04273773

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes