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Dimethyl Sulfoxide → 4-(Propynyloxy)pyridine

HRID 27041
ノート
印刷プレビュー

反応式

HRID 27041 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.CS(C)=O.[CH2:12](Cl)[C:13]#[CH:14]>O.C(=O)([O-])[O-].[Ag+2]>[C:12]([O:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1)#[C:13][CH3:14]
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 679Dimethyl SulfoxideHCID 122213-Chloro-1-propyneHCID 178418642HCID 178418642、化合物

生成物 1

HCID 233434924-(Propynyloxy)pyridine収率 3.6%

試薬・触媒・溶媒 2

HCID 178418647HCID 178418647、化合物触媒HCID 962Water溶媒

実験手順

To a solution of 20.0 g (0.21 mole) 4-hydroxypyridine and 200 ml dimethyl sulfoxide was added 102 g (0.1 mole) silver carbonate. Propargyl chloride (22.5 g, 0.3 mole) was added to this suspension and the mixture heated at 50° for 6 hrs. After cooling to room temperature, the reaction mixture was diluted with water and extracted two times with ether. The combined ether extract was dried, filtered and concentrated as before to give 1.0 g of 4-(propynyloxy)pyridine. The product was 95% pure by vpc. The nmr and ir were compatible with the structure.

後処理

  1. temperaturethe mixture heated at 50° for 6 hrs
  2. extractionextracted two times with ether
  3. extractionThe combined ether extract
  4. customwas dried
  5. filtrationfiltered
  6. concentrationconcentrated as before

出典と根拠

ORDレコード
ord-6a8c1777713940babd8f296f2d89bc27
出典データセット
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04220577

反応ノート

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