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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-(Bis(2-chloroethyl)amino)benzenepropanoic acid → HCID 22096791, 화합물

HRID 1458703
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인쇄 미리보기

반응식

HRID 1458703 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

HCID 22096791HCID 22096791, 화합물

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-0132db4d5f4d461abb07874188aed658
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05852011

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