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Nitric Acid → 4-Formyl-2-methoxy-3-nitrophenyl acetate

HRID 339758
Notes
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Reaction equation

HRID 339758 reaction equation
[C:1]([OH:4])(=[O:3])[CH3:2].[O:5]=[CH:6][C:7]1[CH:15]=[CH:14][C:12](O)=[C:9]([O:10][CH3:11])[CH:8]=1.[N+:16]([O-])([OH:18])=[O:17]>>[C:1]([O:4][C:12]1[CH:14]=[CH:15][C:7]([CH:6]=[O:5])=[C:8]([N+:16]([O-:18])=[O:17])[C:9]=1[O:10][CH3:11])(=[O:3])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 944Nitric AcidHCID 20405942HCID 20405942, compound

Product 1

HCID 2463194-Formyl-2-methoxy-3-nitrophenyl acetateYield 41%

Procedure

Fuming nitric acid (2200 mL) under nitrogen was cooled to 0° C. at which time vanillin acetate (528 g, 2.7 mol) was added portionwise, keeping the internal temperature below 10° C. After 2 h the resulting mixture was poured over ice with stirring. The slurry was filtered and the resulting solids were washed with water (3×100 mL) and air-dried. After 2 days the solids were heated in DCM (3000 mL) until complete dissolution. The solution was allowed to cool to room temperature while hexanes (3000 mL) was added dropwise. The solids were filtered, washed with hexanes (500 mL) and air dried to give 4-formyl-2-methoxy-3-nitrophenyl acetate (269 g, 41%): 1H NMR, (DMSO-d6)□ δ: 9.90 (s, 1H), 7.94 (d, 1H), 7.75 (d, 1H), 3.87 (s, 3H), 2.40 (s, 3H).

Workup

addition
was added portionwise
  • customthe internal temperature below 10° C
  • additionAfter 2 h the resulting mixture was poured over ice
  • filtrationThe slurry was filtered
  • washthe resulting solids were washed with water (3×100 mL)
  • customair-dried
  • temperatureAfter 2 days the solids were heated in DCM (3000 mL) until complete dissolution
  • additionwas added dropwise
  • filtrationThe solids were filtered
  • washwashed with hexanes (500 mL) and air
  • customdried
  • Sources & evidence

    ORD record
    ord-17f3e0f29f75435b93a9cb2c3ca2d6ec
    Source dataset
    uspto-grants-2014_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08895549B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes