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Diethyl Ether → 3-Fluoro-4-trimethylsilylethynylbenzaldehyde

HRID 346264
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인쇄 미리보기

반응식

HRID 346264 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 66111TrimethylsilylacetyleneHCID 27834114-Bromo-3-fluorobenzaldehyde

생성물 1

HCID 199906293-Fluoro-4-trimethylsilylethynylbenzaldehyde

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-c5c33a142b1a4df7a961427205d29c26
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05061726

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