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(3R)-3-hydroxy-3-phenylpropanenitrile → (1R)-3-amino-1-phenylpropan-1-ol

HRID 1760079
Notes
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Reaction equation

HRID 1760079 reaction equation
[C:1]1([C@H:7]([OH:11])[CH2:8][C:9]#[N:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>C1COCC1>[C:1]1([C@H:7]([OH:11])[CH2:8][CH2:9][NH2:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 10130035(3R)-3-hydroxy-3-phenylpropanenitrile

Product 1

HCID 11182697(1R)-3-amino-1-phenylpropan-1-ol

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a THF solution of (R)-3-phenyl-3-hydroxypropanenitrile was slowly added borane dimethyl sulfide complex at room temperature. Methyl sulfide was then distilled from the reaction vessel and the resulting THF solution refluxed for 2.5 h. After cooling to room temperature methanolic HCl was added to the reaction mixture. Methanol and methyl borate were removed by distillation and the reaction mixture neutralized with sodium hydroxide (5N). Extraction of the mixture with dichloromethane followed by concentration provided the crystalline (R)-3-phenyl-3-hydroxypropylamine.

Workup

  1. customat room temperature
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
distillation
Methyl sulfide was then distilled from the reaction vessel
  • temperaturethe resulting THF solution refluxed for 2.5 h
  • additionwas added to the reaction mixture
  • customMethanol and methyl borate were removed by distillation
  • extractionExtraction of the mixture with dichloromethane
  • concentrationfollowed by concentration
  • Sources & evidence

    ORD record
    ord-a0ada6ef4b0b43e88a2d67c69f08646f
    Source dataset
    uspto-grants-2005_01
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06838581B2

    Reaction notes

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