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Dimethyl Disulfide → (2-Fluoro-3-methoxy-5-methylphenyl)(methyl)sulfane

HRID 591441
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HRID 591441 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[O:9][CH3:10].C([Li])(CC)C.[CH3:16][S:17]SC>C1COCC1>[F:1][C:2]1[C:7]([S:17][CH3:16])=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[O:9][CH3:10]
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참가 물질

5

반응물 3

HCID 12232Dimethyl DisulfideHCID 27373722-Fluoro-5-methylanisoleHCID 178418400CID 53628100

생성물 1

HCID 89767603(2-Fluoro-3-methoxy-5-methylphenyl)(methyl)sulfane

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

To a mixture of 1-fluoro-2-methoxy-4-methylbenzene (1.0 g) and THF (dry) (60 mL) was added sec-butyllithium (1.04 mol/L cyclohexane solution, 13.72 mL) dropwise over a period of 20 min at −78° C. After stirring at −78° C. for 20 min, to the mixture was added dimethyl disulfide (1.41 mL) at the same temperature. The mixture was stirred at −78° C. under argon atmosphere for 1 h. The mixture was quenched with saturated aqueous NH4Cl at −78° C. and extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (1.34 g).

후처리

  1. stirringThe mixture was stirred at −78° C. under argon atmosphere for 1 h
  2. customThe mixture was quenched with saturated aqueous NH4Cl at −78° C.
  3. extractionextracted with EtOAc
  4. washThe combined organic layer was washed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by silica gel column chromatography (EtOAc/hexane)

출처 및 근거

ORD 기록
ord-59bc9a1c62cc4837a7ce4f8213a325b2
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09238639B2

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