Sodium Chloride → methyl N-[3-(3,4-dichlorophenyl)benzyl]carbamate

HRID 1168028Notes

Reaction equation

HRID 1168028 reaction equation
Br[C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][CH:13]=1)[CH2:5][NH:6][C:7](=[O:10])[O:8][CH3:9].C(=O)([O-])[O-].[Na+].[Na+].[Cl:20][C:21]1[CH:22]=[C:23](OB(O)O)[CH:24]=[CH:25][C:26]=1[Cl:27].[Cl-].[Na+]>C(O)C.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.C1(C)C=CC=CC=1>[Cl:20][C:21]1[CH:22]=[C:23]([C:2]2[CH:3]=[C:4]([CH:11]=[CH:12][CH:13]=2)[CH2:5][NH:6][C:7](=[O:10])[O:8][CH3:9])[CH:24]=[CH:25][C:26]=1[Cl:27]

Participants

8

Reactant 4

HCID 5234Sodium ChlorideHCID 10340Sodium CarbonateHCID 12090302Methyl (3-bromobenzyl)carbamateHCID 219399273,4-Dichloro-phenyl-boric acid

Product 1

HCID 12090301methyl N-[3-(3,4-dichlorophenyl)benzyl]carbamateYield 94.8%

Reagents, catalysts & solvents 3

HCID 178418397HCID 178418397, compoundCatalystHCID 702EthanolSolventHCID 1140TolueneSolvent

Procedure

1.30 g of methyl N-(3-bromobenzyl)carbamate, 0.56 g of sodium carbonate in aqueous solution (20 ml) and 0.13 g of tetrakis(triphenylphosphine)palladium (0) were added to toluene (40 ml) under a nitrogen atmosphere. The resulting solution was mixed with 1.02 g of 3,4-dichlorophenylboric acid in ethanol (20 ml) at room temperature with stirring and refluxed under heating for 2 hours. After the reaction, the reaction solution was cooled to room temperature, poured into saturated aqueous sodium chloride and extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate and evaporated under reduced pressure for removal of the solvent. The residue was purified by silica gel column chromatography to give 1.45 g of methyl N-[3-(3,4-dichlorophenyl)benzyl]carbamate as a yellow transparent viscous liquid.

Workup

  1. temperaturerefluxed
  2. temperatureunder heating for 2 hours
  3. customAfter the reaction
  4. extractionextracted with ethyl acetate
  5. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  6. customevaporated under reduced pressure for removal of the solvent
  7. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-3e5923a69dfd4da18e8f75f5ae234dfe
Source dataset
uspto-grants-2003_09
Patent number
US06620961B1

Reaction notes

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