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Perchloric Acid → HCID 20036619, 화합물

HRID 1904986
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HRID 1904986 반응식
Cl(O)(=O)(=O)=O.C[O:7][CH:8]=[C:9]([C:14]1[CH:19]=[CH:18][C:17]([C:20]([F:23])([F:22])[F:21])=[CH:16][CH:15]=1)[C:10]([F:13])([F:12])[F:11]>C(OCC)C>[F:21][C:20]([F:22])([F:23])[C:17]1[CH:18]=[CH:19][C:14]([CH:9]([C:10]([F:13])([F:12])[F:11])[CH:8]=[O:7])=[CH:15][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24247Perchloric AcidHCID 538386822-(4-Trifluoromethylphenyl)-3,3,3-trifluoropropenyl methyl ether

생성물 1

HCID 20036619HCID 20036619, 화합물수율 36.3%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Under a nitrogen atmosphere, 10 ml of 70% perchloric acid was added to a solution of 6.1 g of 2-(4-trifluoromethylphenyl)-3,3,3-trifluoropropenyl methyl ether in 20 ml of diethyl ether at 0° to 5° C. The reaction solution was stirred at room temperature for 14 hours. The reaction mixture was poured into ice water and extracted twice with diethyl ether. The ether layers were combined and washed with saturated sodium bisulfate solution and saturated sodium chloride solution successively and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to obtain 2.1 g of the desired crude compound.

후처리

  1. extractionextracted twice with diethyl ether
  2. washwashed with saturated sodium bisulfate solution and saturated sodium chloride solution successively
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-e1d692449b2447c1b174c967d3284c11
출처 데이터셋
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04840971

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