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2-Bromophenol → HCID 15058601、化合物

HRID 2177613
ノート
印刷プレビュー

反応式

HRID 2177613 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[H-].[Na+].Br[CH2:12][CH2:13][F:14]>C1COCC1>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH2:12][CH2:13][F:14]
参加物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 72442-BromophenolHCID 129822-Fluoroethyl bromideHCID 24758Sodium hydride

生成物 1

HCID 15058601HCID 15058601、化合物収率 63%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 2-bromophenol (1.0 g, 5.8 mmol) in THF (20 mL) was add NaH (60%) (462 mg, 11.6 mmol). The reaction mixture was stirred at room temperature for 10 min and then 1-bromo-2-fluoroethane (1.5 g, 11.6 mmol) was added and the mixture was irradiated in a microwave reactor at 130° C. for 40 min. The crude mixture was quenched with H2O and the water layer was extracted with EtOAc. The combined organic layers were dried (Na2SO4), filtered and concentrated. The residue was purified by chromatography on silica gel (0-20% DCM in Heptane) to provide the desired compound as a colorless oil (800 mg, 63%).

後処理

  1. customthe mixture was irradiated in a microwave reactor at 130° C. for 40 min
  2. customThe crude mixture was quenched with H2O
  3. extractionthe water layer was extracted with EtOAc
  4. dry with materialThe combined organic layers were dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by chromatography on silica gel (0-20% DCM in Heptane)

出典と根拠

ORDレコード
ord-d786827193f744f194c191ffa33e82b8
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09066946B2

反応ノート

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