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Dimethylformamide → 4-Azido-2-fluorocyclohexyl 2-phenylethyl ether

HRID 271381
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HRID 271381 반응식
[N-:1]=[N+:2]=[N-:3].[Na+].CN(C)C=O.CS(O[CH:15]1[CH2:20][CH2:19][CH:18]([O:21][CH2:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH:17]([F:30])[CH2:16]1)(=O)=O.C(=O)(O)[O-].[Na+]>C(OCC)(=O)C.CCCCCC>[C:24]1([CH2:23][CH2:22][O:21][CH:18]2[CH2:19][CH2:20][CH:15]([N:1]=[N+:2]=[N-:3])[CH2:16][CH:17]2[F:30])[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1
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참가 물질

7

반응물 4

HCID 6228DimethylformamideHCID 33557Sodium AzideHCID 516892Sodium BicarbonateHCID 725741513-Fluoro-4-(2-phenylethoxy)cyclohexyl methanesulfonate

생성물 1

HCID 725741444-Azido-2-fluorocyclohexyl 2-phenylethyl ether수율 71.3%

시약·촉매·용매 2

HCID 8058
Hexane
용매
HCID 8857Ethyl Acetate용매

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온도
50 °C

실험 절차

Sodium azide (0.500 g, 7.69 mmol) was added to a N,N-dimethylformamide (10 mL) solution of 3-Fluoro-4-(2-phenylethoxy)cyclohexyl methanesulfonate (0.597 g, 1.89 mmol) under nitrogen. The resulting mixture was heated at 50° C. for 24 h, then cooled and poured into saturated sodium bicarbonate. The aqueous mixture was extracted with ethyl acetate (3×) and the combined organic extracts were washed with brine, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. Flash column chromatography (hexane:ethyl acetate, e 90:10) gave 4-Azido-2-fluorocyclohexyl 2-phenylethyl ether as a colorless oil (0.355 g, 71% yield).

후처리

  1. temperaturecooled
  2. extractionThe aqueous mixture was extracted with ethyl acetate (3×)
  3. washthe combined organic extracts were washed with brine
  4. dry with materialdried with anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-81fe9cfaea934dff9d015e01ebe48919
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452893B2

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