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Iodoethane → (3-Bromo-4-fluorophenyl)(ethyl)sulfane

HRID 930893
ノート
印刷プレビュー

反応式

HRID 930893 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([SH:9])[CH:5]=[CH:6][C:7]=1[F:8].[OH-].[Na+].I[CH2:13][CH3:14]>CO>[Br:1][C:2]1[CH:3]=[C:4]([S:9][CH2:13][CH3:14])[CH:5]=[CH:6][C:7]=1[F:8]
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 6340IodoethaneHCID 14798Sodium HydroxideHCID 265970903-Bromo-4-Fluorothiophenol

生成物 1

HCID 86704956(3-Bromo-4-fluorophenyl)(ethyl)sulfane収率 98.5%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
0 °C

実験手順

A mixture of 3-bromo-4-fluorobenzenethiol (3.89 g, 18.79 mmol) and sodium hydroxide (3.95 mL, 19.73 mmol) in MeOH was stirred at 0° C. for 10 minutes. To this solution was added iodoethane (1.803 mL, 22.54 mmol). The reaction mixture was stirred at ambient temperature for 6 hours. The solvent was removed, and the residue was partitioned between water and ethyl acetate. The aqueous layer was extracted with addition ethyl acetate three times. The combined organic layers were washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated to give the title compound (4.35 g, 18.50 mmol, 98% yield). It was used directly for the next reaction.

後処理

  1. stirringThe reaction mixture was stirred at ambient temperature for 6 hours
  2. customThe solvent was removed
  3. customthe residue was partitioned between water and ethyl acetate
  4. extractionThe aqueous layer was extracted with addition ethyl acetate three times
  5. washThe combined organic layers were washed with saturated aqueous sodium chloride
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-20ca365096ac468786d1ce827bda3d91
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09296741B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート