Benzyl Bromide → 4-Bromo-6-chloro-2-methyl-1-benzyloxybenzene

HRID 363104노트

반응식

HRID 363104 반응식
[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([OH:9])=[C:4]([CH3:10])[CH:3]=1.[CH2:11](Br)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([O:9][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:4]([CH3:10])[CH:3]=1

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 820314-Bromo-6-chloro-o-cresol

생성물 1

HCID 185046304-Bromo-6-chloro-2-methyl-1-benzyloxybenzene수율 90%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of 50 g of 4-bromo-6-chloro-2-methylphenol and 42.5 g of benzyl bromide dissolved in 200 ml of N,N-dimethylformamide was stirred at room temperature, to which 37.4 g of potassium carbonate was added, and the mixture was stirred for 12 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure, and the residue was added to 400 ml of diethyl ether, washed with water, dried with anhydrous magnesium sulfate, and concentrated to obtain a crude product. The crude product was subjected to silica gel chromatography, which afforded 63 g of 4-bromo-6-chloro-2-methyl-1-benzyloxybenzene (90% yield).

후처리

  1. additionwas added
  2. customAfter completion of the reaction
  3. customthe solvent was removed by distillation under reduced pressure
  4. additionthe residue was added to 400 ml of diethyl ether
  5. washwashed with water
  6. dry with materialdried with anhydrous magnesium sulfate
  7. concentrationconcentrated
  8. customto obtain a crude product

출처 및 근거

ORD 기록
ord-b2c7d625e14b45bf9a8c41ad2155fec3
출처 데이터셋
uspto-grants-1999_02
특허 번호
US05872137

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