Dichloromethane → Methyl 2-(benzamido)-4-bromobenzoate

HRID 1673333Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1673333
[C:1](Cl)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(Cl)Cl.[NH2:13][C:14]1[CH:23]=[C:22]([Br:24])[CH:21]=[CH:20][C:15]=1[C:16]([O:18][CH3:19])=[O:17]>C(N(CC)CC)C>[C:1]([NH:13][C:14]1[CH:23]=[C:22]([Br:24])[CH:21]=[CH:20][C:15]=1[C:16]([O:18][CH3:19])=[O:17])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

5

Edukt 3

HCID 6344DichloromethaneHCID 7412Benzoyl chlorideHCID 17871390Methyl 2-Amino-4-bromobenzoate

Produkt 1

HCID 57879335Methyl 2-(benzamido)-4-bromobenzoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8471TriethylamineLösungsmittel

Versuchsvorschrift

0.55 mL of benzoyl chloride was added to 10 mL of a methylene chloride solution containing 1.0 g of methyl 2-amino-4-bromobenzoate and 0.73 mL of triethylamine while ice-cooled and stirred at room temperature for 1 hour. The solvent was evaporated under reduced pressure and a saturated sodium hydrogen carbonate aqueous solution and ethyl acetate were added to the residue. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with 1.0 mol/L hydrochloric acid and a saturated sodium chloride aqueous solution sequentially, and the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the obtained residue and a solid substance was separated by filtration to obtain 0.9 g of methyl 2-(benzamido)-4-bromobenzoate as while solid.

Aufarbeitung

  1. temperaturecooled
  2. customThe solvent was evaporated under reduced pressure
  3. additiona saturated sodium hydrogen carbonate aqueous solution and ethyl acetate were added to the residue
  4. customThe organic layer was separated
  5. dry with materialdried over anhydrous magnesium sulfate
  6. washafter washed with 1.0 mol/L hydrochloric acid
  7. customa saturated sodium chloride aqueous solution sequentially, and the solvent was evaporated under reduced pressure
  8. additionDiisopropyl ether was added to the obtained residue
  9. customa solid substance was separated by filtration

Quellen und Nachweise

ORD-Eintrag
ord-fc73191ca8d94b36a200685105b8b6e2
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US07999132B2

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