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Ethyl Acetate → HCID 58566366, 화합물

HRID 1876393
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HRID 1876393 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:13]([OH:15])=[O:14])[C:5]2[O:9][C:8]([CH3:11])([CH3:10])[CH2:7][C:6]=2[CH:12]=1.S(OOS([O-])(=O)=O)([O-])(=O)=[O:17].[K+].[K+].C(#N)C.O.C(OCC)(=O)C>O>[Cl:1][C:2]1[CH:3]=[C:4]([C:13]([OH:15])=[O:14])[C:5]2[O:9][C:8]([CH3:11])([CH3:10])[C:7](=[O:17])[C:6]=2[CH:12]=1
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참가 물질

6

반응물 4

HCID 8857Ethyl AcetateHCID 24412Potassium PersulfateHCID 101769185-Chloro-2,2-dimethyl-2,3-dihydrobenzofuran-7-carboxylic acidHCID 18373917Acetonitrile--water (1/1)

생성물 1

HCID 58566366HCID 58566366, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of 5-chloro-2,2-dimethyl-2,3-dihydrobenzofuran-7-carboxylic acid (654) (2.39 g, 10.5 mmol), potassium persulfate (8.55 g, 31.6 mmol), cupric sulfate pentahydrate (2.62 g, 10.5 mmol) and acetonitrile/water (1:1) (90 mL) were heated at reflux for 1 hour. Ethyl acetate and water were added and the layers separated. The aqueous phase was extracted with ethyl acetate and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide 5-chloro-2,2-dimethyl-3-oxo-2,3-dihydrobenzofuran-7-carboxylic acid (655) as a yellow solid.

후처리

  1. temperatureat reflux for 1 hour
  2. customthe layers separated
  3. extractionThe aqueous phase was extracted with ethyl acetate
  4. dry with materialthe combined organic layers were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-35e4a2af12754a1191bac5f50a0428a9
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08309600B2

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