5-(4-Chlorophenyl)-2-methylphenylboronic acid → HCID 178476525, compound

HRID 1430743Notes

Reaction equation

HRID 1430743 reaction equation
[C:1]([O-:4])(=[O:3])[CH3:2].[C:5]([O-:8])(=[O:7])[CH3:6].[C:9]([O-:12])(=[O:11])[CH3:10].C([O-])(=O)C.[Pb+4:17].[Cl:18][C:19]1[CH:34]=[CH:33][C:22]([C:23]2[CH:24]=[CH:25][C:26]([CH3:32])=[C:27](B(O)O)[CH:28]=2)=[CH:21][CH:20]=1>>[C:1]([O-:4])(=[O:3])[CH3:2].[C:5]([O-:8])(=[O:7])[CH3:6].[C:9]([O-:12])(=[O:11])[CH3:10].[Cl:18][C:19]1[CH:34]=[CH:33][C:22]([C:23]2[CH:24]=[CH:25][C:26]([CH3:32])=[C:27]([Pb+3:17])[CH:28]=2)=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 594459235-(4-Chlorophenyl)-2-methylphenylboronic acidHCID 178418268HCID 178418268, compound

Product 1

HCID 178476525HCID 178476525, compound

Conditions

Temperature
40 °C

Procedure

To a mixture of lead tetraacetate (2.44 g, 5.50 mmol) and mercuric diacetate (0.16 g, 0.50 mmol), thoroughly flushed with nitrogen, is added anhydrous chloroform (6 ml). This mixture is warmed to 40° C., and 4′-chloro-4-methylbiphen-3-ylboronic acid (1.23 g, 5.00 mmol) is added in one portion, and the suspension is heated at this temperature for 5 hours. After cooling to room temperature the mixture is concentrated to a small volume, then triturated with hexanes and filtered to yield crude 4′-chloro-4-methylbiphen-3-yllead triacetate.

Workup

  1. customthoroughly flushed with nitrogen
  2. additionis added anhydrous chloroform (6 ml)
  3. temperaturethe suspension is heated at this temperature for 5 hours
  4. temperatureAfter cooling to room temperature the mixture
  5. concentrationis concentrated to a small volume
  6. customtriturated with hexanes
  7. filtrationfiltered

Sources & evidence

ORD record
ord-bed70f5edb3c404ca3479c02b3cbce20
Source dataset
uspto-grants-2015_01
Patent number
US08940913B2

Reaction notes

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