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Acetic Acid → 5-Benzoxazoleacetic acid, 2-phenyl-

HRID 2398746
Notes
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Reaction equation

HRID 2398746 reaction equation
OC([C:5]1[CH:6]=[CH:7][C:8]2[O:12][C:11]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[N:10][C:9]=2[CH:19]=1)C#N.C.[C:21]([OH:24])(=[O:23])[CH3:22]>[Pd]>[C:13]1([C:11]2[O:12][C:8]3[CH:7]=[CH:6][C:5]([CH2:22][C:21]([OH:24])=[O:23])=[CH:19][C:9]=3[N:10]=2)[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 176Acetic AcidHCID 297MethaneHCID 21434017HCID 21434017, compound

Product 1

HCID 379285-Benzoxazoleacetic acid, 2-phenyl-

Reagents, catalysts & solvents 1

HCID 23938PalladiumCatalyst

Procedure

A solution of α-hydroxy-2-phenyl-5-benzoxazolyl-acetonitrile (2 g.) in acetic acid (30 ml.) containing palladium or charcoal was hydrogenated for 4 hours. The catalyst was filtered off and the solution was evaporated to dryness. The residue was recrystallised to give pure 2-phenyl-5-benzoxazolylacetic acid m.p. 175° C.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. filtrationThe catalyst was filtered off
  2. customthe solution was evaporated to dryness
  3. customThe residue was recrystallised

Sources & evidence

ORD record
ord-ace5b03aa5ab4d35906bed6526170fa3
Source dataset
uspto-grants-1977_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04025636

Reaction notes

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