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Hydrochloric Acid → 4-Aminocyclopent-2-ene-1-carboxylic acid

HRID 1492075
Notes
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Reaction equation

HRID 1492075 reaction equation
[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[C:3](=[O:8])[NH:2]2.Cl.C(OCC)(=[O:12])C>C(O)C>[NH2:2][C@@H:1]1[CH2:7][C@H:4]([C:3]([OH:8])=[O:12])[CH:5]=[CH:6]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 8857Ethyl AcetateHCID 5486782-Azabicyclo(2.2.1)hept-5-en-3-one

Product 1

HCID 100346434-Aminocyclopent-2-ene-1-carboxylic acidYield 61.2%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To 4.58 g (42 mmol) of (±)-2-azabicyclo[2.2.1]hept-5-en-3-one, 190 ml of 1N hydrochloric acid was added, and the mixture was refluxed for 2 hours with heating. The solvent was evaporated, and the resulting white crystals were washed with 30 ml of acetone, followed by drying to give 6.59 g of crude crystals of the subject (+)ACP acid. This crude crystals were dissolved in ethanol (20 ml) with heating, and thereafter ethyl acetate (85 ml) was added to the resulting solution, followed by cooling to room temperature. The crystals thus deposited were filtrated to give 4.26 g (25.7 mmol; yield: 61.2%) of the subject (+)ACP acid (melting point: 169-172° C.).

Workup

  1. temperaturethe mixture was refluxed for 2 hours
  2. temperaturewith heating
  3. customThe solvent was evaporated
  4. washthe resulting white crystals were washed with 30 ml of acetone
  5. customby drying
  6. customto give 6.59 g of crude crystals of the subject (+)ACP acid
  7. temperaturewith heating
  8. filtrationThe crystals thus deposited were filtrated

Sources & evidence

ORD record
ord-496560b51f204c7ea0807dbfdbb64643
Source dataset
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05371282

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes