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Ethanol → HCID 86245030, compound

HRID 1171884
Notes
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Reaction equation

HRID 1171884 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[CH2:11][C:12]([OH:14])=[O:13].S(=O)(=O)(O)O.[CH2:20](O)[CH3:21]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[CH2:11][C:12]([O:14][CH2:20][CH3:21])=[O:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 687671652-Bromo-5-nitrobenzeneacetic acid

Product 1

HCID 86245030HCID 86245030, compound

Procedure

A mixture composed of 5.21 g (20 mmol) of (2-bromo-5-nitrophenyl)acetic acid (Zhumal Organicheskoi Khimii (1974) 10, 92-5), 80 ml of absolute ethanol and 0.1 ml of concentrated sulfuric acid is refluxed for 6 hours. After cooling, the reaction medium is concentrated under vacuum and taken up in ether. This organic phase is washed with saturated NaHCO3 solution and then with water, after which it is dried over Na2SO4. After concentrating under vacuum, 5.54 g of a beige solid are obtained.

Workup

  1. temperature
is refluxed for 6 hours
  • temperatureAfter cooling
  • concentrationthe reaction medium is concentrated under vacuum
  • washThis organic phase is washed with saturated NaHCO3 solution
  • dry with materialwith water, after which it is dried over Na2SO4
  • concentrationAfter concentrating under vacuum, 5.54 g of a beige solid
  • customare obtained
  • Sources & evidence

    ORD record
    ord-a0acd240f22f4725a8b2ef91f5abc032
    Source dataset
    uspto-grants-2010_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07829721B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes