Water → 2-Phenylterephthalic acid mono methyl ester

HRID 1532828Notes

Reaction equation

HRID 1532828 reaction equation
[CH3:1][O:2][C:3](=[O:17])[C:4]1[CH:9]=[CH:8][C:7](Br)=[CH:6][C:5]=1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.CCN(CC[O:25][C:26]1C=CC(CC2C=CC=CC=2)=CC=1)CC.Cl.[C]=[O:41].O>CN(C=O)C.CC([O-])=O.CC([O-])=O.[Pd+2]>[CH3:1][O:2][C:3](=[O:17])[C:4]1[CH:9]=[CH:8][C:7]([C:26]([OH:25])=[O:41])=[CH:6][C:5]=1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Participants

7

Reactant 4

HCID 962WaterHCID 175534Tesmilifene HydrochlorideHCID 54332024Methyl 5-bromo-[1,1'-biphenyl]-2-carboxylateHCID 178418416HCID 178418416, compound

Product 1

HCID 857324742-Phenylterephthalic acid mono methyl ester

Reagents, catalysts & solvents 2

HCID 167845palladium(II) acetateCatalystHCID 6228DimethylformamideSolvent

Procedure

A solution of 4-bromo-2-phenylbenzoic acid methyl ester (1.0 equivalent), Pd(OAc)2 (0.05 equivalent) and DPPE (1.0 equivalent) is heated in DMF to 65° C. under 4 atm. of carbon monoxide until TLC analysis indicates that the reaction is complete. The reaction mixture is poured into water and extracted with ethyl acetate which is dried and evaporated. The product is purified by chromatography on silica gel.

Workup

  1. extractionextracted with ethyl acetate which
  2. customis dried
  3. customevaporated
  4. customThe product is purified by chromatography on silica gel

Sources & evidence

ORD record
ord-bcd4b97899f04a25800c13125ec66453
Source dataset
uspto-grants-2001_03
Patent number
US06204293B1

Reaction notes

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