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Potassium Carbonate → HCID 21187897, 화합물

HRID 356968
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HRID 356968 반응식
[F:1][C:2]1([F:20])[C:5]([O:6][C:7]2[CH:8]=[C:9]([CH:14]=[CH:15][C:16]=2[O:17][CH3:18])[C:10]([O:12]C)=[O:11])=[CH:4][C:3]1=[CH2:19].C(=O)([O-])[O-].[K+].[K+]>CO.O>[F:1][C:2]1([F:20])[C:5]([O:6][C:7]2[CH:8]=[C:9]([CH:14]=[CH:15][C:16]=2[O:17][CH3:18])[C:10]([OH:12])=[O:11])=[CH:4][C:3]1=[CH2:19]
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참가 물질

5

반응물 2

HCID 11430Potassium CarbonateHCID 21187923HCID 21187923, 화합물

생성물 1

HCID 21187897HCID 21187897, 화합물

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

A solution of methyl 3-(4,4-difluoro-3-methylenecyclobut-1-enyloxy)-4-methoxybenzoate (1.39 g) in methanol (22 mL) is treated with a solution of potassium carbonate (0.83 g) in water (8 mL) and the solution is heated at 60°-70° C. for 8 hours, cooled and evaporated. The residue is dissolved in water (30 mL), extracted with diethyl ether (50 mL) and acidified to pH 4 by treatment with glacial acetic acid. The precipitated solid is extracted with ethyl acetate (2×75 mL). The combined organic extracts are dried over magnesium sulfate and concentrated, to give 3-(4,4-difluoro-3-methylene- cyclobut-1-enyloxy)-4-methoxybenzoic acid, in the form of a white solid, m.p. 163°-165° C.

후처리

  1. temperaturethe solution is heated at 60°-70° C. for 8 hours
  2. temperaturecooled
  3. customevaporated
  4. dissolutionThe residue is dissolved in water (30 mL)
  5. extractionextracted with diethyl ether (50 mL)
  6. extractionThe precipitated solid is extracted with ethyl acetate (2×75 mL)
  7. dry with materialThe combined organic extracts are dried over magnesium sulfate
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-485c3f92dbb24527aa941da817c05d52
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05840724

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