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Nitric Acid → 2-Chloro-3-formyl-6-methoxy-5-nitrophenyl acetate

HRID 274484
Notes
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Reaction equation

HRID 274484 reaction equation
[C:1]([O:4][C:5]1[C:10]([O:11][CH3:12])=[CH:9][CH:8]=[C:7]([CH:13]=[O:14])[C:6]=1[Cl:15])(=[O:3])[CH3:2].[N+:16]([O-])([OH:18])=[O:17]>>[C:1]([O:4][C:5]1[C:10]([O:11][CH3:12])=[C:9]([N+:16]([O-:18])=[O:17])[CH:8]=[C:7]([CH:13]=[O:14])[C:6]=1[Cl:15])(=[O:3])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 944Nitric AcidHCID 144509932-Chloro-3-formyl-6-methoxyphenyl acetate

Product 1

HCID 144509942-Chloro-3-formyl-6-methoxy-5-nitrophenyl acetate

Procedure

38 g of 2-chloro-3-formyl-6-methoxyphenyl acetate are introduced portionwise at -5° to -10° within 15 minutes into 150 ml of 98 percent nitric acid. After stirring at -5° for 30 minutes the reaction mixture is poured into 1.5 1 of ice-water and extracted three times with 500 ml of methylene chloride. The combined organic phases are washed with ice-water, dried over sodium sulfate and evaporated. The residue is crystallized from ether. There is obtained 2-chloro-3-formyl-6-methoxy-5-nitrophenyl acetate of m.p. 84°-85°.

Workup

  1. extractionextracted three times with 500 ml of methylene chloride
  2. washThe combined organic phases are washed with ice-water
dry with material
dried over sodium sulfate
  • customevaporated
  • customThe residue is crystallized from ether
  • Sources & evidence

    ORD record
    ord-8c97e3c6ce9e41ec87326e1763f39304
    Source dataset
    uspto-grants-1995_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05389653

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes