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Ammonium Hydroxide → 1,2-Difluoronaphthalene

HRID 2182109
ノート
印刷プレビュー

反応式

HRID 2182109 の反応式
[F:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](F)=[C:4](F)[C:3]=1[F:14].BrC1C=C2C(=CC=1)C(F)(F)C(F)(F)C=C2.[NH4+].[OH-]>C1COCC1.[Zn]>[F:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[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

6

反応物 3

HCID 14923Ammonium HydroxideHCID 123439521,2,3,4-TetrafluoronaphthaleneHCID 224834376-Bromo-1,1,2,2-tetrafluoro-1,2-dihydronaphthalene

生成物 1

HCID 111374671,2-Difluoronaphthalene収率 95%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 8028Tetrahydrofuran
溶媒

実験手順

A solution of the tetrafluoro naphthalene, 6-bromo-1,1,2,2-tetrafluoro-1,2-dihydronaphthalene (4.74 g, 16.80 mmol) in THF (15 ml) was treated with 30% aqueous NH4OH (30 ml) and zinc (8.45 g, 130 mmol) and stirred under N2 for 24 hours at RT. The reaction was monitored by GC/MS for disappearance of the starting material and found to be complete. The solution was filtered, extracted with hexane (30 ml), and filtered through a short silica column (20 g). The hexane solution was evaporated in vacuo to afford an oil. This crystallized on cooling to room temperature to afford 2.62 g (95% yield) of product.

後処理

  1. filtrationThe solution was filtered
  2. extractionextracted with hexane (30 ml)
  3. filtrationfiltered through a short silica column (20 g)
  4. customThe hexane solution was evaporated in vacuo
  5. customto afford an oil
  6. customThis crystallized
  7. temperatureon cooling to room temperature

出典と根拠

ORDレコード
ord-3b03b91615c44d2cb19f899240417f06
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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