Water → HCID 19045659, compound

HRID 232891Notes

Reaction equation

HRID 232891 reaction equation
[F:1][C:2]([F:23])([F:22])[C:3]([N:5]1[CH2:10][CH2:9][CH2:8][CH2:7][C:6]21[CH2:19][CH2:18][C:17]1[C:12](=[CH:13][CH:14]=[C:15]([O:20][CH3:21])[CH:16]=1)[CH2:11]2)=[O:4].[N+:24]([O-:27])([O-:26])=[O:25].[NH4+].FC(F)(F)C(OC(=O)C(F)(F)F)=O.O>C(Cl)(Cl)Cl>[F:23][C:2]([F:1])([F:22])[C:3]([N:5]1[CH2:10][CH2:9][CH2:8][CH2:7][C:6]21[CH2:19][CH2:18][C:17]1[C:12](=[CH:13][C:14]([N+:24]([O-:26])=[O:25])=[C:15]([O:20][CH3:21])[CH:16]=1)[CH2:11]2)=[O:4].[F:23][C:2]([F:1])([F:22])[C:3]([N:5]1[CH2:10][CH2:9][CH2:8][CH2:7][C:6]21[CH2:19][CH2:18][C:17]1[C:12](=[CH:13][CH:14]=[C:15]([O:20][CH3:21])[C:16]=1[N+:24]([O-:27])=[O:25])[CH2:11]2)=[O:4]

Participants

7

Procedure

6.0 g of 1'-trifluoroacetyl-3,4-dihydro-6-methoxyspiro[naphthalene-2(1H),2'-piperidine] was dissolved in 150 ml of chloroform. After 1.5 g of ammonium nitrate was suspended in this solution, 9 ml of trifluoroacetic anhydride was added, followed by overnight stirring at room temperature. After water was added, the reaction mixture was extracted with methylene chloride. The extract was dried over anhydrous sodium sulfate and filtered, after which the solvent was distilled off. The residue was purified by silica gel column chromatography to yield 1.4 g of 1'-trifluoroacetyl-3,4-dihydro-6-methoxy-7-nitrospiro[naphthalene-2(1H),2'-piperidine] and 0.457 g of 1'-trifluoroacetyl-3,4-dihydro-6-methoxy-5-nitrospiro[naphthalene-2(1H),2'-piperidine].

Workup

  1. additionwas added
  2. extractionthe reaction mixture was extracted with methylene chloride
  3. dry with materialThe extract was dried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. distillationafter which the solvent was distilled off
  6. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-a3a2d3fccaf24222b123a7b4c3d59ea6
Source dataset
uspto-grants-1997_01
Patent number
US05591849

Reaction notes

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