Propyne → Phthalic Anhydride

HRID 2164855

Reaktionsgleichung

Reaktionsgleichung von HRID 2164855
C[C:2]12[CH2:11][CH2:10][CH2:9][CH2:8][CH:7]1[C:6](=[O:12])[O:5][C:3]2=[O:4].C(C1CC(=O)OC1=O)=CCCCCCCCCCC.CC#C>>[C:6]1(=[O:12])[O:5][C:3](=[O:4])[C:2]2=[CH:11][CH:10]=[CH:9][CH:8]=[C:7]12

Komponenten

4

Edukt 3

HCID 6335PropyneHCID 329333-(1-Dodecen-1-yl)dihydro-2,5-furandioneHCID 3016472Methylhexahydrophthalic anhydride

Produkt 1

HCID 6811Phthalic Anhydride

Versuchsvorschrift

The procedures of Example 1 were repeated except that 38.2 g. of methylhexahydrophthalic anhydride (Example 2) and 61.2 g. of dodecenylsuccinic anhydride (Example 3) which was a maleinization product of propylene tetramer or butylene trimer, were employed, respectively, instead of 34 g. of phthalic anhydride, to give light yellow resins. The properties thereof are shown in Table 1.

Quellen und Nachweise

ORD-Eintrag
ord-bf0250d297b14922ad23662d06f7e4b0
Quelldatensatz
uspto-grants-1985_03
Patentnummer
US04507376

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