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5-Fluoroindanone oxime → 5-Fluoro-2,3-dihydro-1H-inden-1-amine

HRID 375600
Notes
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Reaction equation

HRID 375600 reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[N:11]O)[CH2:6][CH2:5]2>C(O)(=O)C.[Zn]>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH:7]([NH2:11])[CH2:6][CH2:5]2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 736055205-Fluoroindanone oxime

Product 1

HCID 166663285-Fluoro-2,3-dihydro-1H-inden-1-amineYield 96.3%

Reagents, catalysts & solvents 2

HCID 23994ZincCatalystHCID 176Acetic AcidSolvent

Procedure

Zinc powder (20.2 g) was added during three hours to the stirred solution of the above oxime (20.2 g) in acetic acid (200 ml) which maintains the temperature at 25°-35° C. The resulting mixture was stirred an additional 12 hours at room temperature. The solids were removed by filtration and the filtrate concentrated in vacuo. The concentrated filtrate was partitioned between water and toluene and the aqueous phase adjusted to pH 12 with ammonium hydroxide and extracted with toluene. Solvent removal in vacuo gave 5-fluoro-1-aminoindan (17.8 g) as a colored oil.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. customat 25°-35° C
  2. customThe solids were removed by filtration
  3. concentrationthe filtrate concentrated in vacuo
  4. customThe concentrated filtrate was partitioned between water and toluene
  5. extractionextracted with toluene
  6. customSolvent removal in vacuo

Sources & evidence

ORD record
ord-308f788b92cc49588ca4ad24af84b0b0
Source dataset
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05486541

Reaction notes

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