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Potassium Acetate → 4-Chloro-2-(difluoromethoxy)phenol

HRID 2178126
ノート
印刷プレビュー

反応式

HRID 2178126 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5](Br)=[C:4]([O:9][CH:10]([F:12])[F:11])[CH:3]=1.C([O-])(=[O:15])C.[K+].OOS([O-])=O.[K+]>C1COCC1.CCOC(C)=O.O.C(OCC)C.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:15])=[C:4]([O:9][CH:10]([F:12])[F:11])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 3

HCID 517044Potassium AcetateHCID 222953811-Bromo-4-chloro-2-(difluoromethoxy)benzeneHCID 23707502Potassium hydroxy sulfite

生成物 1

HCID 600510324-Chloro-2-(difluoromethoxy)phenol

試薬・触媒・溶媒 5

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)触媒
HCID 962
Water
溶媒
3 回
HCID 3283Diethyl Ether溶媒
HCID 8028Tetrahydrofuran溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of 4-chloro-2-(difluoromethoxy)bromobenzene (Preparation 27, 200 mg, 0.63 mmol) in THF (6 mL) was added bis-neopentylglycolatodiboron (149 mg, 0.660 mmol), potassium acetate (191 mg, 1.88 mmol) and Pd(dppf)Cl2 (23 mg, 0.031 mmol). The reaction mixture was heated to reflux for 4 hours before cooling and diluting with EtOAc and water. The organic layer was collected, washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was dissolved in acetone (6 mL) and treated with a solution of oxone (1.64 g, 2.54 mmol) in water (6 mL). The reaction mixture was stirred at room temperature for 15 minutes. The reaction mixture was diluted with diethyl ether (10 mL) and water (5 mL). The organic layer was collected, washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified using silica gel column chromatography eluting with 0-15% diethyl ether in DCM to afford the title compound.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 4 hours
  3. temperaturebefore cooling
  4. customThe organic layer was collected
  5. washwashed with brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. dissolutionThe residue was dissolved in acetone (6 mL)
  9. customThe organic layer was collected
  10. washwashed with brine
  11. dry with materialdried over Na2SO4
  12. concentrationconcentrated in vacuo
  13. customThe residue was purified
  14. washeluting with 0-15% diethyl ether in DCM

出典と根拠

ORDレコード
ord-3e0d3f3b75c640f580e90c4fb4df631f
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09067922B2

反応ノート

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