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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Ethanol → HCID 178479647、化合物

HRID 2296349
ノート
印刷プレビュー

反応式

HRID 2296349 の反応式
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][NH2:6].[ClH:7].C(=N)(OCC)[CH:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)O.[CH2:21]([OH:23])C>>[ClH:7].[OH:23][C:21]1[N:1]([CH2:9][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5][N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 702EthanolHCID 1045PutrescineHCID 12387918Ethyl 1-hydroxy-1-phenylmethanecarboximidate hydrochloride

生成物 1

HCID 178479647HCID 178479647、化合物収率 34%

実験手順

To 200 ml of absolute ethanol was added 1,4-diaminobutane at 0° C. with continuous stirring. To this solution waas added an equal molar amount of ethyl mandelimidate hydrochloride. After stirring at 0°-5° C. for two hours, the suspension was heated under reflux 12 hours then cooled and concentrated to remove any traces of NH3. The concentrated solution was acidified by dropwise addition of ethanolic HCl into the suspension which was then concentrated to dryness and the residue recrystallized several times from CH3CN/ether to yield 14.5 g (34%) of product: mp 179°-181° C. Structure was confirmed by IR and NMR.

後処理

  1. temperaturethe suspension was heated
  2. temperatureunder reflux 12 hours
  3. temperaturethen cooled
  4. concentrationconcentrated
  5. customto remove any traces of NH3
  6. additionThe concentrated solution was acidified by dropwise addition of ethanolic HCl into the suspension which
  7. concentrationwas then concentrated to dryness
  8. customthe residue recrystallized several times from CH3CN/ether

出典と根拠

ORDレコード
ord-cadabf6a12a44235b18e58b934466783
出典データセット
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04428948

反応ノート

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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