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Maleic Anhydride → Di(3-pentynyl) maleate

HRID 617099
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인쇄 미리보기

반응식

HRID 617099 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-d6dd2a74bc284fa5b6904002ee56bf57
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05948339

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