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

HRID 591441
ノート
印刷プレビュー

反応式

HRID 591441 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-59bc9a1c62cc4837a7ce4f8213a325b2
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09238639B2

反応ノート

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