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Maleic Anhydride → Di(3-pentynyl) maleate

HRID 582224
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인쇄 미리보기

반응식

HRID 582224 반응식
[CH2:1]([OH:6])[CH2:2][C:3]#[C:4][CH3:5].[C:7]1(=[O:13])[O:12][C:10](=[O:11])[CH:9]=[CH:8]1>C1(C)C=CC=CC=1.CS(O)(=O)=O>[C:10]([O:12][CH2:5][CH2:4][C:3]#[C:2][CH3:1])(=[O:11])/[CH:9]=[CH:8]\[C:7]([O:6][CH2:1][CH2:2][C:3]#[C:4][CH3:5])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7923Maleic AnhydrideHCID 662953-Pentyn-1-ol

생성물 1

HCID 86754233Di(3-pentynyl) maleate

시약·촉매·용매 2

HCID 6395Methanesulfonic Acid촉매HCID 1140Toluene용매

실험 절차

15 g of 3-pentyn-1-ol was reacted with 8.35 g of maleic anhydride in 25 ml of toluene and in the presence of one drop of methanesulfonic acid. 11.5 g of DPTNM was isolated from the reaction mixture (bp=134-140° C./full vacuum GC purity=98.8 %). 1H NMR data: 1.77 (t, J=3 Hz, CH3), 2.52 (m, CH2CC), 4.22 (t, J=7 Hz, CH2 -O), 6.22 (s, maleate olefin CHs).

후처리

  1. custom11.5 g of DPTNM was isolated from the reaction mixture (bp=134-140° C./full vacuum GC purity=98.8 %)

출처 및 근거

ORD 기록
ord-f1fe69a1321f41b5a23df5e4aff5185d
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05922795

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