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Hydroxyamine hydrochloride → HCID 72363102, compound

HRID 1363189
Notes
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Reaction equation

HRID 1363189 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[O:10][CH2:9][CH2:8][C:7]2=O.Cl.[NH2:14][OH:15].C([O-])(=O)C.[Na+]>>[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[O:10][CH2:9][CH2:8][C:7]2=[N:14][OH:15]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 139538178-Fluoro-2,3-dihydro-4H-1-benzopyran-4-one

Product 1

HCID 72363102HCID 72363102, compound

Procedure

A round bottom flask was charged with 8-fluorochroman-4-one (8.2 g), hydroxylamine hydrochloride (3.78 g) and sodium acetate (4.46 g). A reflux condenser was added, the flask was purged with argon, dry EtOH (20 mL) was added, and the mixture was stirred at reflux for 18 hours. The solution was cooled to room temperature, diluted with EtOAc, and washed with water. The organic phase was dried, and evaporated to give the intermediate 8-fluorochroman-4-one oxime, which was reduced with Raney Nickel in EtOH at 50 PSI to yield the titled amine (4.69 g, 57%).

Workup

  1. additionA reflux condenser was added
  2. customthe flask was purged with argon, dry EtOH (20 mL)
  3. additionwas added
  4. temperatureat reflux for 18 hours
  5. additiondiluted with EtOAc
  6. washwashed with water
  7. customThe organic phase was dried
  8. customevaporated

Sources & evidence

ORD record
ord-1a2f824b0c3642268bbc8ece70fb7277
Source dataset
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07884109B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes