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Hydrochloric Acid → HCID 86742529, 화합물

HRID 2231850
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HRID 2231850 반응식
C([O:3][C:4](=O)/[CH:5]=[CH:6]/[CH2:7][CH2:8][C:9]([F:12])([F:11])[F:10])C.[H-].C([Al+]CC(C)C)C(C)C.Cl>C(OCC)C.CCCCCC>[F:10][C:9]([F:12])([F:11])[CH2:8][CH2:7][CH2:6]/[CH:5]=[CH:4]/[OH:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 21225700DiisobutylaluminumhydrideHCID 21666955HCID 21666955, 화합물

생성물 1

HCID 86742529HCID 86742529, 화합물

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8058Hexane용매

실험 절차

A solution of 10 g of 6,6,6-trifluoro-2-transhexenoic acid ethyl ester (see above) in 70 ml of diethyl ether is cooled to 0°-5° and at this temperature 102 ml of 1M diisobutylaluminium hydride solution in hexane are added. The reaction mixture is then stirred for 5 minutes at 0°-5° and carefully hydrolysed with approx. 200 ml of 6N hydrochloric acid. The organic phase is separated off and the aqueous phase is extracted a further 3 times with ether. The combined organic phases are dried over MgSO4, and concentrated by evaporation. Chromatography of the residue on silica gel with hexane/ethyl acetate (7:3) yields the title compound in the form of a colourless liquid.

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후처리

  1. additionare added
  2. customThe organic phase is separated off
  3. extractionthe aqueous phase is extracted a further 3 times with ether
  4. dry with materialThe combined organic phases are dried over MgSO4
  5. concentrationconcentrated by evaporation

출처 및 근거

ORD 기록
ord-c07d6dc8578b48c38804bc602fec6b8d
출처 데이터셋
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04785004

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