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Water → 1-(4'-Trifluoromethyl-biphenyl-4-yl)-heptan-1-ol

HRID 1669333
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HRID 1669333 반응식
[CH2:1]([Mg]Br)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[F:9][C:10]([F:26])([F:25])[C:11]1[CH:16]=[CH:15][C:14]([C:17]2[CH:22]=[CH:21][C:20]([CH:23]=[O:24])=[CH:19][CH:18]=2)=[CH:13][CH:12]=1.O.[Cl-].[Na+]>O1CCCC1.C(OCC)(=O)C>[F:9][C:10]([F:25])([F:26])[C:11]1[CH:12]=[CH:13][C:14]([C:17]2[CH:22]=[CH:21][C:20]([CH:23]([OH:24])[CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])=[CH:19][CH:18]=2)=[CH:15][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 5234Sodium ChlorideHCID 27827124'-(Trifluoromethyl)-4-biphenylcarbaldehydeHCID 178444609HCID 178444609, 화합물

생성물 1

HCID 597294131-(4'-Trifluoromethyl-biphenyl-4-yl)-heptan-1-ol수율 73%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran
용매
HCID 8857Ethyl Acetate용매

실험 절차

Add hexyl magnesium bromide (2.0M in ethyl ether, 8 mL, 16 mmol) to 4′-trifluoromethyl-biphenyl-4-carbaldehyde (2.0 g, 8 mmol) (prepared in a manner substantially similar to preparation 25, or other methods known in the art) in tetrahydro-furan (30 mL) at 0° C. under inert atmosphere. Stir 1.5 hours. Quench reaction with saturated solution of ammonium chloride, dilute with ethyl acetate. Wash organic phase with water then saturated sodium chloride solution. Dry organic fraction with Na2SO4, filter, and concentrate under reduced pressure. Purify on silica gel chromatography (0-30% Ethyl acetate/hexanes gradient) to provide 1.95 g of title compound (73%).

후처리

  1. customprepared in a manner substantially similar to preparation 25, or other methods
  2. customat 0° C.
  3. customQuench
  4. customreaction with saturated solution of ammonium chloride
  5. filtrationDry organic fraction with Na2SO4, filter
  6. concentrationconcentrate under reduced pressure
  7. customPurify on silica gel chromatography (0-30% Ethyl acetate/hexanes gradient)

출처 및 근거

ORD 기록
ord-d8c67ec133334ab4a89ec726ce5197cb
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07989457B2

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