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2-(2-Chloro-4-fluorophenyl)acetamide → 2-(2-Chloro-4-fluorophenyl)ethan-1-amine

HRID 1048084
Notes
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Reaction equation

HRID 1048084 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][C:10]([NH2:12])=O.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][NH2:12]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 27737162-(2-Chloro-4-fluorophenyl)acetamideHCID 21226445Aluminium lithium hydride

Product 1

HCID 218881112-(2-Chloro-4-fluorophenyl)ethan-1-amineYield 16.2%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
0 °C

Procedure

2-(2-chloro-4-fluorophenyl)acetamide (400 mg, 2.13 mmol) was diluted with THF (2 mL), placed under nitrogen and cooled to 0° C. LAH (4264 μL, 4.26 mmol) was added dropwise and the reaction was refluxed for 3 hours. The reaction was cooled to 0° C. and quenched with 160 μL of water, 160 μL of 15% NaOH, and 530 μL of water. After stirring for 30 minutes the reaction was filtered and concentrated. The material was purified using a biotage 25 column eluting with 2% NH4OH/10% methanol/DCM to yield 2-(2-chloro-4-fluorophenyl)ethanamine (60 mg, 0.346 mmol, 16.2% yield).

Workup

  1. temperaturethe reaction was refluxed for 3 hours
  2. temperatureThe reaction was cooled to 0° C.
  3. customquenched with 160 μL of water, 160 μL of 15% NaOH, and 530 μL of water
  4. filtrationwas filtered
  5. concentrationconcentrated
  6. customThe material was purified
  7. washeluting with 2% NH4OH/10% methanol/DCM

Sources & evidence

ORD record
ord-831d5b2a77864753bfaa346b756966fc
Source dataset
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08569522B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes