Ethyl Acetate → 2'-Chloro-[1,1'-biphenyl]-2-carbaldehyde

HRID 1394154

Reaction equation

HRID 1394154 reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[Cl:8].[CH:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1B(O)O)=[O:10].C(=O)([O-])[O-].[Na+].[Na+].C(OCC)(=O)C>C1(C)C=CC=CC=1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[Cl:8])=[O:10]

Participants

7

Reactant 4

HCID 8857Ethyl AcetateHCID 10340Sodium CarbonateHCID 127541-Bromo-2-chlorobenzeneHCID 2921892-Formylphenylboronic acid

Product 1

HCID 13923752'-Chloro-[1,1'-biphenyl]-2-carbaldehyde

Reagents, catalysts & solvents 2

HCID 178418397HCID 178418397, compoundCatalystHCID 1140TolueneSolvent

Procedure

To a solution of 2-bromochlorobenzene (0.12 mL, 1 mmol) and 2-formylbenzeneboronic acid (0.17 g, 1.1 mmol) in toluene (9 mL) were added 2M aq. sodium carbonate (1.2 mL) followed by (Ph3P)4Pd (0.34 g, 0.3 mmol). The resulting reaction mixture was refluxed for 3 h, cooled and diluted ethyl acetate. The organic phase was washed with water, saturated aq. sodium bicarbonate, brine and dried over sodium sulfate. The filtrate was concentrated in vacuo and the residue obtained was purified by chromatography (hexane:ethyl acetate; 4:1) to yield the title product.

Workup

  1. customThe resulting reaction mixture
  2. temperaturewas refluxed for 3 h
  3. temperaturecooled
  4. washThe organic phase was washed with water, saturated aq. sodium bicarbonate, brine
  5. dry with materialdried over sodium sulfate
  6. concentrationThe filtrate was concentrated in vacuo
  7. customthe residue obtained
  8. customwas purified by chromatography (hexane:ethyl acetate; 4:1)

Sources & evidence

ORD record
ord-c2a9002fd6a140cba829b5dc2899c98a
Source dataset
uspto-grants-2008_03
Patent number
US07348348B2

Linked notes

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