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Water → 5,6-Difluoro-2-bromonaphthalene

HRID 2182115
ノート
印刷プレビュー

反応式

HRID 2182115 の反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](F)([F:12])[C:7](F)([F:14])[CH:6]=[CH:5]2.O.O.O.O.O.O.[OH-].C[N+](C)(C)C>[Zn].C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([F:12])=[C:7]([F:14])[CH:6]=[CH:5]2
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 82620Tetramethylammonium Hydroxide PentahydrateHCID 224834376-Bromo-1,1,2,2-tetrafluoro-1,2-dihydronaphthalene

生成物 1

HCID 114138325,6-Difluoro-2-bromonaphthalene

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 8028Tetrahydrofuran溶媒

実験手順

Zinc (0.89 g, 14 mmol) was added to a stirred mixture of 2.4 g (8.7 mmol) of 6-bromo-1,1,2,2-tetrafluoro-1,2-dihydronaphthalene, 4 ml of water, 6 ml of THF, and 7.6 g of tetramethylammonium hydroxide pentahydrate that was cooled in an ice bath. The mixture was allowed to warm to room temperature. After 2 hours, the zinc was filtered, and the phases were separated. The aqueous layer was extracted three times with hexanes. The combined organic phase was washed three times with brine, stirred over MgSO4 and activated carbon for 3 hours, and then stored for 15 hours. The MgSO4 and carbon were filtered off, and the solvent was removed under vacuum. A colorless solid (1.9 g, 7.7 mmol, 89%) remained.

後処理

  1. temperaturewas cooled in an ice bath
  2. filtrationthe zinc was filtered
  3. customthe phases were separated
  4. extractionThe aqueous layer was extracted three times with hexanes
  5. washThe combined organic phase was washed three times with brine
  6. waitstored for 15 hours
  7. filtrationThe MgSO4 and carbon were filtered off
  8. customthe solvent was removed under vacuum

出典と根拠

ORDレコード
ord-f0c7692a60744734a4a37d5cff267ef0
出典データセット
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06894200B2

反応ノート

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