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Maleic Anhydride → 6-Maleimido-1-hexanol

HRID 2306122
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반응식

HRID 2306122 반응식
[C:1]1(=[O:7])[O:6][C:4](=O)[CH:3]=[CH:2]1.[NH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][OH:15]>C(O)(=O)C>[OH:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][N:8]1[C:1](=[O:7])[CH:2]=[CH:3][C:4]1=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7923Maleic AnhydrideHCID 199606-Amino-1-hexanol

생성물 1

HCID 121937996-Maleimido-1-hexanol

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

One mole equivalent of maleic anhydride and one mole equivalent of 6-amino hexanol are dissolved in anhydrous acetic acid and the solution is heated under reflux for eight hours. The acetic acid is distilled off in a rotary evaporator. The residue is dissolved in diethyl ether and washed once with 1 N NaOH, and twice with water. After drying over MgSO4 and evaporating the diethyl ether, the residue is crystallized from isopropyl ether to produce N-(6-hydroxyhexyl) maleimide.

후처리

  1. temperaturethe solution is heated
  2. temperatureunder reflux for eight hours
  3. distillationThe acetic acid is distilled off in a rotary evaporator
  4. dissolutionThe residue is dissolved in diethyl ether
  5. washwashed once with 1 N NaOH
  6. dry with materialAfter drying over MgSO4
  7. customevaporating the diethyl ether
  8. customthe residue is crystallized from isopropyl ether

출처 및 근거

ORD 기록
ord-55e5aa71184643d3a2b45f40104d61bb
출처 데이터셋
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06441213B1

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