HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Water → HCID 69067984, compound

HRID 1726381
Notes
Print preview

Reaction equation

HRID 1726381 reaction equation
[C:1]1([C:7]2[O:8][C:9]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[CH:10][C:11]=2[C:12]#N)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH2:20].[OH-:21].[Na+]>C(O)CO>[C:1]1([C:7]2[O:8][C:9]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[CH:10][C:11]=2[C:12]([OH:21])=[O:20])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 27421802,5-Diphenylfuran-3-carbonitrile

Product 1

HCID 69067984HCID 69067984, compound

Reagents, catalysts & solvents 1

HCID 174Ethylene GlycolSolvent

Procedure

A suspension of 2,5-diphenylfuran-3-carbonitrile (0.87 g, 3.56 mmol) in ethylene glycol and 3M NaOH (10 ml) was heated at reflux for 3 days. Water was added to the reaction mixture and extracted into CH2Cl2. The organic layer was dried with MgSO4, filtered and concentrated to provide 2,5-diphenylfuran-3-carboxylic acid (intermediate XXVIf, 900 mg) as white solid.

Workup

  1. temperaturewas heated
  2. temperatureat reflux for 3 days
  3. extractionextracted into CH2Cl2
  4. dry with materialThe organic layer was dried with MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-f3213b59182c4e2b82865e4edc8b0ada
Source dataset
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07491821B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes