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Diethyl Ether → 3-Fluoro-4-trimethylsilylethynylbenzaldehyde

HRID 346264
ノート
印刷プレビュー

反応式

HRID 346264 の反応式
Br[C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][C:3]=1[F:10].[CH3:11][Si:12]([C:15]#[CH:16])([CH3:14])[CH3:13].C(OCC)C>C(N(CC)CC)C>[F:10][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:2]=1[C:16]#[C:15][Si:12]([CH3:14])([CH3:13])[CH3:11])[CH:6]=[O:7]
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 3283Diethyl EtherHCID 66111TrimethylsilylacetyleneHCID 27834114-Bromo-3-fluorobenzaldehyde

生成物 1

HCID 199906293-Fluoro-4-trimethylsilylethynylbenzaldehyde

試薬・触媒・溶媒 1

HCID 8471Triethylamine溶媒

実験手順

To a stirred solution of 4-bromo-3-fluorobenzaldehyde (6 g) in triethylamine (60 ml) was added trimethylsilylacetylene (4.6 ml), bis-triphenylphosphinepalladium dichloride (331 mg) and cuprous iodide (130 mg). The resulting mixture was allowed to stir overnight at room temperature under a nitrogen atmosphere. After this time, diethyl ether was added and the mixture was filtered. The filtrate was washed with water and brine before drying over anhydrous magnesium sulphate and evaporation in vacuo. The resulting oil was crystallised from cold hexane to give 3-fluoro-4-trimethylsilylethynylbenzaldehyde as a light brown solid (4 g).

後処理

  1. filtrationthe mixture was filtered
  2. washThe filtrate was washed with water and brine
  3. dry with materialbefore drying over anhydrous magnesium sulphate and evaporation in vacuo
  4. customThe resulting oil was crystallised from cold hexane

出典と根拠

ORDレコード
ord-c5c33a142b1a4df7a961427205d29c26
出典データセット
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05061726

反応ノート

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