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Hydrazine hydrate (1:1) → (2S)-2-(4-Fluorophenyl)propan-1-amine

HRID 2276739
Notes
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Reaction equation

HRID 2276739 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([CH3:21])[CH2:9][N:10]2C(=O)C3C(=CC=CC=3)C2=O)=[CH:4][CH:3]=1.O.NN>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C@H:8]([CH3:21])[CH2:9][NH2:10])=[CH:6][CH:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24654Hydrazine hydrate (1:1)HCID 67453498(S)-2-(2-(4-Fluorophenyl)propyl)isoindoline-1,3-dione

Product 1

HCID 28267524(2S)-2-(4-Fluorophenyl)propan-1-amineYield 100.2%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Conditions

Temperature
80 °C

Procedure

To a room-temperature solution of (S)-2-(2-(4-fluorophenyl)propyl)isoindoline-1,3-dione (900 mg, 3.2 mmol, 1.0 equiv) in toluene (14 mL) was added hydrazine hydrate (1.4 mL, 45 mmol, 14 equiv) by syringe. The resulting mixture was heated to 80° C. for 30 minutes and then cooled to room temperature. The resulting solution was decanted from the solid in the reaction mixture, and the solid was washed with additional toluene. The combined organic layers were combined and concentrated in vacuo to provide the title compound (491 mg, 99%), which was used without further purification.

Workup

  1. temperaturecooled to room temperature
  2. customThe resulting solution was decanted from the solid in the reaction mixture
  3. washthe solid was washed with additional toluene
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-623998cec767480fbf85f2f631c5d2e7
Source dataset
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09133123B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes