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(2S)-2-amino-2-cyclopentylacetic acid → (2S)-2-Amino-2-cyclopentylethan-1-ol

HRID 539083
Notes
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Reaction equation

HRID 539083 reaction equation
[NH2:1][C@@H:2]([CH:6]1[CH2:10][CH2:9][CH2:8][CH2:7]1)[C:3](O)=[O:4].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[NH2:1][C@@H:2]([CH:6]1[CH2:10][CH2:9][CH2:8][CH2:7]1)[CH2:3][OH:4]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 10374564(2S)-2-amino-2-cyclopentylacetic acidHCID 21226445Aluminium lithium hydride

Product 1

HCID 55283839(2S)-2-Amino-2-cyclopentylethan-1-ol

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a stirred solution of (S)-2-amino-2-cyclopentylacetic acid (1.00 g, 6.98 mmol) in THF (20 mL) was added dropwise a solution of LiAlH4 in THF (1.0 M, 10.5 mL, 10.5 mmol) at 0° C. under N2. The reaction was allowed to warm to ambient temperature and heated at reflux overnight. After cooling, the reaction mixture was cooled to 0° C. and carefully quenched by dropwise addition of water (0.4 mL) followed by 15% NaOH solution (0.4 mL) and water (1.2 mL). The mixture was stirred at ambient temperature for 15 minutes and filtered through Celite. The filtrate was concentrated to give crude (S)-2-amino-2-cyclopentylethanol, which was used in the next step without further purification.

Workup

  1. temperatureheated
  2. temperatureat reflux overnight
  3. temperatureAfter cooling
  4. temperaturethe reaction mixture was cooled to 0° C.
  5. customcarefully quenched by dropwise addition of water (0.4 mL)
  6. filtrationfiltered through Celite
  7. concentrationThe filtrate was concentrated

Sources & evidence

ORD record
ord-3cb664679bbe4c53b79f6abc3bd5c2e2
Source dataset
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08865726B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes