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1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 23044549、化合物

HRID 2165280
ノート
印刷プレビュー

反応式

HRID 2165280 の反応式
O.[Cl:2][CH2:3][CH:4]=[O:5].[N+:6]([CH2:8][C:9]([NH2:11])=[O:10])#[C-:7].N12CCCN=C1CCCCC2>CO>[Cl:2][CH2:3][CH:4]1[O:5][CH:7]=[N:6][CH:8]1[C:9]([NH2:11])=[O:10]
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 3

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 12227820Acetaldehyde, chloro-, hydrateHCID 206649162-Isocyanoacetamide

生成物 1

HCID 23044549HCID 23044549、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

114 g of chloroacetaldehyde monohydrate, and 84 g of isocyanoacetamide were dissolved in 1000 ml of methanol. The mixture was cooled to 0°-3° C. and a solution of 38 g of 1,8-diazabicyclo[5.4.0]undec-7-ene in 200 ml of methanol was added with string. At this temperature. stirring was continued for 30 minutes, and, after removal of the cooling bath, for an additional hour. The solvent was removed in vacuo and the residue refluxed twice with 1000 ml each time of ethyl acetate. The combined hot extracts were treated with charcoal, filtered while still hot and evaporated to yield the title compound as a crystalline residue, melting point 110°-112° C. after recrystallization from ethyl acetate.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureThe mixture was cooled to 0°-3° C.
  2. customafter removal of the cooling bath
  3. waitfor an additional hour
  4. customThe solvent was removed in vacuo
  5. temperaturethe residue refluxed twice with 1000 ml each time of ethyl acetate
  6. additionThe combined hot extracts were treated with charcoal
  7. filtrationfiltered while still hot and
  8. customevaporated

出典と根拠

ORDレコード
ord-4e793792b70d4cb1a6a430f6d00d0bca
出典データセット
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04939253

反応ノート

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