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Hydrochloric Acid → HCID 10997097、化合物

HRID 1761722
ノート
印刷プレビュー

反応式

HRID 1761722 の反応式
[CH2:1]([N:4]([C:9]([O:11]C)=O)[C:5](=O)[CH2:6][NH2:7])[C:2]#[CH:3].[OH-:13].[Na+].Cl>CO>[CH2:1]([N:4]1[CH2:5][C:6](=[O:13])[NH:7][C:9]1=[O:11])[C:2]#[CH:3]
参加物反応条件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 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 21242407HCID 21242407、化合物

生成物 1

HCID 10997097HCID 10997097、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
70 °C

実験手順

2.0 g of N-propargyl-N-methoxycarbonylglycinamide were added to the mixture of 5 ml of methanol and 2.5 ml of 20% aqueous solution of sodium hydroxide and maintained at 70° C. for an hour. After cooled down to room temperature; the reaction mixture was neutralized with concentrated hydrochloric acid followed by concentrating and drying the same by an evaporation under reduced pressure. Then it was extracted with acetonitrile and sodium chloride was removed off from the extract by filtration. The solvent was evaporated off from the filtrate to obtain 1.4 g of 1-propargyl-2,4-dioxoimidazolidine (melting point: 124°-125° C.).

後処理

  1. temperatureAfter cooled down to room temperature
  2. concentrationby concentrating
  3. customdrying the
  4. customsame by an evaporation under reduced pressure
  5. extractionThen it was extracted with acetonitrile and sodium chloride
  6. customwas removed off from the
  7. extractionextract by filtration
  8. customThe solvent was evaporated off from the filtrate

出典と根拠

ORDレコード
ord-f05c517ad5bc4a8baf1a6ee67ce0ad6f
出典データセット
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04827020

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート