Hydroxyamine hydrochloride → HCID 73997431, compound

HRID 1415182Notes

Reaction equation

HRID 1415182 reaction equation
[CH3:1][C:2]1([CH:15]=O)[C:7]2[NH:8][C:9]3[C:14]([C:6]=2[CH2:5][CH2:4][O:3]1)=[CH:13][CH:12]=[CH:11][CH:10]=3.Cl.[NH2:18][OH:19].C([O-])(=O)C.[Na+]>CO>[CH3:1][C:2]1([CH:15]=[N:18][OH:19])[C:7]2[NH:8][C:9]3[C:14]([C:6]=2[CH2:5][CH2:4][O:3]1)=[CH:13][CH:12]=[CH:11][CH:10]=3

Participants

5

Reactant 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 22766917HCID 22766917, compound

Product 1

HCID 73997431HCID 73997431, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A solution of 1-methyl-1,3,4,9-tetrahydropyrano [3,4-b] -indole-1-carboxaldehyde (547 mg), described in Example 777, aqueous hydroxylamine hydrochloride (2.5 ml of 5N) and aqueous sodium acetate (2.5 ml of 5N) and methanol (5 ml) is heated at 50° - 60° C. for 5 min. and then kept at 4° C. for 16 hr. The precipitate is collected and recrystallized from ethanol water to afford 1-methyl-1,3,4,9-tetrahydropyrano [3,4-b]indole-1-carboxaldehyde oxime, m.p. 176° - 178° C.

Workup

  1. temperatureis heated at 50° - 60° C. for 5 min.
  2. customThe precipitate is collected
  3. customrecrystallized from ethanol water

Sources & evidence

ORD record
ord-23284ad69b8d4de58a18d3aae827a64a
Source dataset
uspto-grants-1977_01
Patent number
US04003913

Reaction notes

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