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Chloroacetonitrile → 2-Ethoxy-4-hydroxythiazole-5-carbonitrile

HRID 329194
ノート
印刷プレビュー

反応式

HRID 329194 の反応式
Cl[CH2:2][C:3]#[N:4].[K].[C:6]([NH:11][C:12](=[S:16])[O:13][CH2:14][CH3:15])(OCC)=[O:7].C(N(CC)CC)C>CO>[C:3]([C:2]1[S:16][C:12]([O:13][CH2:14][CH3:15])=[N:11][C:6]=1[OH:7])#[N:4]
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 4

HCID 7856ChloroacetonitrileHCID 8471TriethylamineHCID 3457746Ethyl ethoxythiocarbonylcarbamateHCID 5462222Potassium

生成物 1

HCID 214389692-Ethoxy-4-hydroxythiazole-5-carbonitrile

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

22.8 g of chloroacetonitrile were added dropwise with stirring at room temperature to a suspension of 61.5 g of the potassium salt of ethyl N-carbethoxy-thiocarbamate [described by Guha et al, Indian Chem. Soc., Vol. 6 (1929), p. 570] in one liter of methanol and after stirring the mixture for 2 hours, 30 g of triethylamine were added thereto. The mixture was stirred for another 48 hours and was then refluxed for 2 hours and filtered. The filtrate was concentrated to dryness and the residue was added to sodium hydroxide solution. The resulting solution was washed with ethyl ether, acidified with hydrochloric acid and extracted with ethyl ether. The extracts were dried and evaporated to dryness and the residue was crystallized from petroleum ether to obtain 26.4 g of 5-cyano-4-hydroxy-2-ethoxy-thiazole melting at 132°C.

後処理

  1. stirringThe mixture was stirred for another 48 hours
  2. temperaturewas then refluxed for 2 hours
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated to dryness
  5. additionthe residue was added to sodium hydroxide solution
  6. washThe resulting solution was washed with ethyl ether
  7. extractionextracted with ethyl ether
  8. customThe extracts were dried
  9. customevaporated to dryness
  10. customthe residue was crystallized from petroleum ether

出典と根拠

ORDレコード
ord-aa30dbd7d66042cb93b7310e3bb5c8b4
出典データセット
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04020076

反応ノート

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