Sodium Hydroxide → 4-Bromo-3,5-diethoxybenzoic acid

HRID 38480노트

반응식

HRID 38480 반응식
[Br:1][C:2]1[C:11]([O:12][CH2:13][CH3:14])=[CH:10][C:5]([C:6]([O:8]C)=[O:7])=[CH:4][C:3]=1[O:15][CH2:16][CH3:17].[OH-].[Na+]>C1COCC1.CO>[Br:1][C:2]1[C:11]([O:12][CH2:13][CH3:14])=[CH:10][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[O:15][CH2:16][CH3:17]

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 57930905Methyl 4-bromo-3,5-diethoxybenzoate

생성물 1

HCID 579309874-Bromo-3,5-diethoxybenzoic acid

시약·촉매·용매 2

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of methyl 4-bromo-3,5-diethoxybenzoate (3.00 g) in a mixture of THF (25 ml) and MeOH (10 ml) was added aqueous 1N NaOH (20 ml) and the reaction mixture was stirred at room temperature for 6 h. The mixture was concentrated under reduced pressure and the residue was diluted with H2O and diethylether. The aqueous layer was acidified with aqueous 1N HCl, the mixture was extracted with CHCl3 and dried over sodium sulfate. After filtration and concentration, the residue was dried in vacuo to give the crude intended compound as a colorless solid. Thus obtained crude product was used in the next step without further purification.

후처리

  1. concentrationThe mixture was concentrated under reduced pressure
  2. additionthe residue was diluted with H2O and diethylether
  3. extractionthe mixture was extracted with CHCl3
  4. dry with materialdried over sodium sulfate
  5. filtrationAfter filtration and concentration
  6. customthe residue was dried in vacuo
  7. customto give the crude
  8. customThus obtained crude product
  9. customwas used in the next step without further purification

출처 및 근거

ORD 기록
ord-a47a94cc5a9e4777ab1d821f29080afe
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08524730B2

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