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2-Butene-1,4-diol → 4-(4-Fluoro-3-methylbenzyloxy)but-2-en-1-ol

HRID 1361058
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HRID 1361058 반응식
[H-].[Na+].[CH2:3]([OH:8])[CH:4]=[CH:5][CH2:6][OH:7].Br[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([F:17])=[C:13]([CH3:18])[CH:12]=1>C1COCC1>[F:17][C:14]1[CH:15]=[CH:16][C:11]([CH2:10][O:7][CH2:6][CH:5]=[CH:4][CH2:3][OH:8])=[CH:12][C:13]=1[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80652-Butene-1,4-diolHCID 24758Sodium hydrideHCID 27781354-(Bromomethyl)-1-fluoro-2-methylbenzene

생성물 1

HCID 669684504-(4-Fluoro-3-methylbenzyloxy)but-2-en-1-ol수율 49.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a suspension of NaH (1.0 g, 60% oil dispersion) in 80 mL THF was slowly added but-2-ene-1,4-diol (2.0 g, 22 mmol) as a solution in 5 mL THF at room temperature. To this mixture was added dropwise 4-bromomethyl-1-fluoro-2-methyl-benzene (5.0 g, 24 mmol) and the resulting stirred for 8 h at room temperature. The reaction was quenched by the slow addition of 50 mL of saturated NH4Cl and the mixture extracted with ethyl acetate (3×80 mL). The combined organic layers were washed with brine (2×60 mL) and dried over sodium sulfate. The solvent was removed under reduced pressure and the product isolated by Flash column chromatography eluting with 0% to 50% ethyl acetate/hexane to give 2.3 g of the title compound as a light yellow oil.

후처리

  1. customat room temperature
  2. customThe reaction was quenched by the slow addition of 50 mL of saturated NH4Cl
  3. extractionthe mixture extracted with ethyl acetate (3×80 mL)
  4. washThe combined organic layers were washed with brine (2×60 mL)
  5. dry with materialdried over sodium sulfate
  6. customThe solvent was removed under reduced pressure
  7. customthe product isolated by Flash column chromatography
  8. washeluting with 0% to 50% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-a71af59c488f46bbb5b017e3fb44970c
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879911B2

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