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Potassium Carbonate → HCID 57565950, 화합물

HRID 1728167
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HRID 1728167 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:10])=[C:6]([CH:9]=1)[CH:7]=[O:8].Br[CH2:12][CH2:13][O:14][C:15](=[O:17])[CH3:16].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH2:12][CH2:13][O:14][C:15](=[O:17])[CH3:16])=[C:6]([CH:7]=[O:8])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 124815-Chloro-salicylaldehydeHCID 135641-Acetoxy-2-bromoethane

생성물 1

HCID 57565950HCID 57565950, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

5-Chloro-2-hydroxy-benzaldehyde (2 g, 12.8 mmol), acetic acid 2-bromo-ethyl ester (2.57 g, 15.4 mmol), K2CO3 (5.3 g, 38.5 mmol) and KI (0.26 g, 1.54 mmol) were mixed in DMF (20 mL). Then the reaction tube was placed into the cavity of a focused monomode microwave reactor and the contents of the flask were irradiated at 130° C. for 30 min. The mixture was filtered and the filtrate was concentrated. The residue was dissolved in CH2Cl2 and the organic layer was washed with water for several times. Then the organic layer was dried over anhydrous Na2SO4 and concentrated to obtain a yellow solid. (2.7 g)

후처리

  1. customThen the reaction tube was placed into the cavity of a focused monomode microwave reactor
  2. customthe contents of the flask were irradiated at 130° C. for 30 min
  3. filtrationThe mixture was filtered
  4. concentrationthe filtrate was concentrated
  5. dissolutionThe residue was dissolved in CH2Cl2
  6. washthe organic layer was washed with water for several times
  7. dry with materialThen the organic layer was dried over anhydrous Na2SO4
  8. concentrationconcentrated
  9. customto obtain a yellow solid

출처 및 근거

ORD 기록
ord-91dab68b39774aecadcbe31ac2cca493
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07495007B2

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