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Potassium Carbonate → Benzene, 1-chloro-4-ethynyl-

HRID 1199595
ノート
印刷プレビュー

反応式

HRID 1199595 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[C:9][Si](C)(C)C)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+]>CO.CCCCCC>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[CH:9])=[CH:4][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

5

反応物 2

HCID 11430Potassium CarbonateHCID 3337298(4-Chlorophenylethynyl)trimethylsilane

生成物 1

HCID 70118Benzene, 1-chloro-4-ethynyl-

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8058Hexane溶媒

実験手順

To a solution of 2(4-chlorophenyl)-1-trimethylsilylethyne Prepared in Stage 1 (30.90g:0.02 mole) in methanol was added potassium carbonate (0.276g:002 mole). The mixture was stirred at room temperature until starting material disappeared as monitored by gas liquid chromatography. After this time, solvent was removed in vacuo and the residue taken up in dichloromethane. The solution was dried and declourised over charcoal. Filtration, followed by removal of solvent gave a brown solid which was passed through silica in hexane. This gave pale yellow crystals (1.511g:55.3%)

後処理

  1. customAfter this time, solvent was removed in vacuo
  2. customThe solution was dried
  3. filtrationFiltration
  4. customfollowed by removal of solvent
  5. customgave a brown solid which

出典と根拠

ORDレコード
ord-04cdcb925b3b4ffb92883ea9d746ec49
出典データセット
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04902332

反応ノート

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