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4-(Bis(2-chloroethyl)amino)benzenepropanoic acid → HCID 22096791、化合物

HRID 1458703
ノート
印刷プレビュー

反応式

HRID 1458703 の反応式
[Cl:1][CH2:2][CH2:3][N:4]([C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][C:16]([OH:18])=O)=[CH:10][CH:9]=1)[CH2:5][CH2:6][Cl:7].C(Cl)(=O)C([Cl:22])=O>ClCCCl>[Cl:1][CH2:2][CH2:3][N:4]([C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][C:16]([Cl:22])=[O:18])=[CH:10][CH:9]=1)[CH2:5][CH2:6][Cl:7]
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 2

HCID 231984-(Bis(2-chloroethyl)amino)benzenepropanoic acidHCID 65578Oxalyl chloride

生成物 1

HCID 22096791HCID 22096791、化合物

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

3-[4-[N,N-Bis(2-chloroethyl)amino]phenyl]propionic acid (0.24 g; 0.83 mmol) was dissolved in 5 ml of 1,2-dichloroethane, followed by the dropwise addition of 0.22 ml (2.58 mmol; 3.1 equivalents) of oxalyl chloride (with ice-cooling from an intermediary time point due to violent exotherm). After completion of the dropwise addition, the temperature of the resultant mixture was allowed to rise again to room temperature, at which the mixture was stirred for 3 hours and then allowed to stand overnight. The mixture was thereafter concentrated under reduced pressure, whereby the title compound was obtained in a crude form. The crude compound was provided for use in the next reaction without purification.

後処理

  1. temperaturecooling from an intermediary time point due to violent exotherm)
  2. additionAfter completion of the dropwise addition
  3. customto rise again to room temperature, at which
  4. waitto stand overnight
  5. concentrationThe mixture was thereafter concentrated under reduced pressure, whereby the title compound
  6. customwas obtained in a crude form

出典と根拠

ORDレコード
ord-0132db4d5f4d461abb07874188aed658
出典データセット
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05852011

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