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Sodium Hydroxide → HCID 3730311, compound

HRID 2373860
Notes
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Reaction equation

HRID 2373860 reaction equation
[OH-:1].[Na+].[F:3][C:4]([F:21])([F:20])[C:5]1[CH:6]=[CH:7][C:8]([O:11][C:12]2[CH:19]=[CH:18][C:15]([CH:16]=[O:17])=[CH:14][CH:13]=2)=[N:9][CH:10]=1>[N+]([O-])([O-])=O.[Ag+]>[F:21][C:4]([F:20])([F:3])[C:5]1[CH:6]=[CH:7][C:8]([O:11][C:12]2[CH:19]=[CH:18][C:15]([C:16]([OH:1])=[O:17])=[CH:14][CH:13]=2)=[N:9][CH:10]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 269857004-((5-(Trifluoromethyl)pyridin-2-yl)oxy)benzaldehyde

Product 1

HCID 3730311HCID 3730311, compound

Reagents, catalysts & solvents 1

HCID 24470Silver NitrateCatalyst

Conditions

Temperature
0 °C

Procedure

To aq. NaOH (3.2 g, 80 mmol) was added silver nitrate (3.4 g, 40 mmol) and stirred for 10 min., then the mixture was cooled to 0° C. and the above aldehyde (4.62 g, 17 mmol) was added. The mixture was stirred overnight, then filtrate through celite. The filtrate was collected and acidified with conc. HCl. The solid was collected by filtration and dried under vacuum to give 4-(5-trifluoromethyl-pyridin-2-yloxy)-benzoic acid. (3.5 g)

Workup

  1. stirringThe mixture was stirred overnight
  2. customThe filtrate was collected
  3. filtrationThe solid was collected by filtration
  4. customdried under vacuum

Sources & evidence

ORD record
ord-56dbedb3370f41c3a4f0fa4d71cea5b6
Source dataset
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07459472B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes