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Bromine → 5-Bromo-2-ethylbenzaldehyde

HRID 2389696
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HRID 2389696 반응식
[CH2:1]([C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH:5]=[O:6])[CH3:2].[Al+3].[Cl-].[Cl-].[Cl-].[Br:15]Br>C(Cl)Cl>[Br:15][C:8]1[CH:9]=[CH:10][C:3]([CH2:1][CH3:2])=[C:4]([CH:7]=1)[CH:5]=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24408BromineHCID 1234062-EthylbenzaldehydeHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 547723895-Bromo-2-ethylbenzaldehyde

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A stirred suspension of 2-ethylbenzaldehyde (0.98 mL, 7.45 mmol) and AlCl3 (1.74 g, 13 mmol) in DCM (4.5 mL) at 0° C. is treated with a solution of Br2 (0.38 mL, 7.45 mmol) in DCM (4.5 mL) dropwise over 6 h then stirred 16 h at RT. After this time, the reaction mixture is poured over ice-water (50 mL), the layers separated and the aqueous layer extracted with DCM (3×50 mL). The organic phases are combined and washed with 2M HCl (100 mL), aqueous NaHCO3 (100 mL) and brine (100 mL), dried over Na2SO4 then the solvents removed in vacuo. Purification by column chromatography (gradient elution—100% heptane increasing to 10% EtOAc in heptane) gives the title compound.

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후처리

  1. customthe layers separated
  2. extractionthe aqueous layer extracted with DCM (3×50 mL)
  3. washwashed with 2M HCl (100 mL), aqueous NaHCO3 (100 mL) and brine (100 mL)
  4. dry with materialdried over Na2SO4
  5. customthe solvents removed in vacuo
  6. customPurification
  7. washby column chromatography (gradient elution—100% heptane increasing to 10% EtOAc in heptane)

출처 및 근거

ORD 기록
ord-3997b46c88c94175bff54c21c88b77de
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273747B2

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