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

HRID 409345
Notes
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Reaction equation

HRID 409345 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.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 9321HydrazineHCID 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 (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 concentrated in vacuo to provide the title compound (491 mg, 99%), which was used without further purification. m/z=154.2 [M+H]+.

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. concentrationThe combined organic layers were concentrated in vacuo

Sources & evidence

ORD record
ord-0c88d2bcc2d348c9bed38be25465d7b3
Source dataset
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08759380B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes