1-Dodecanol → L-lactide epsilon-caprolactone

HRID 399684

Reaktionsgleichung

Reaktionsgleichung von HRID 399684
C(O)CCCCCCCCCCC.[CH3:14][CH2:15][CH2:16][CH2:17][CH:18]([C:21]([O-:23])=[O:22])[CH2:19]C.CCC[CH2:27][CH:28]([C:31]([O-:33])=[O:32])CC.[Sn+2]>>[C:21]1(=[O:23])[O:22][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]1.[CH3:27][C@@H:28]1[O:23][C:21](=[O:22])[C@H:18]([CH3:19])[O:33][C:31]1=[O:32]

Komponenten

3

Edukt 2

HCID 81931-DodecanolHCID 93182-ethylhexanoic acid tin(II) salt

Produkt 1

HCID 131710947L-lactide epsilon-caprolactone

Versuchsvorschrift

The procedure in Example 1 was substantially repeated, except that 13.6 mL of 1-dodecanol instead of 4.00 mL of glycerol and 0.12 mL (40 pmol) instead of 0.10 mL of stannous octoate solution were used. The copolymer was dried under vacuum (0.1 mm Hg) at 110° C. for about 16 hours to remove any unreacted monomer. The copolymer had an inherent viscosity of 0.15 dL/g in HFIP at 25° C. The copolymer was viscous liquid at room temperature. The molar ratio of PCL/PLA was found to be 51.5/48.5 by proton NMR.

Aufarbeitung

  1. customThe copolymer was dried under vacuum (0.1 mm Hg) at 110° C. for about 16 hours
  2. customto remove any unreacted monomer
  3. customat 25° C
  4. customat room temperature

Quellen und Nachweise

ORD-Eintrag
ord-2d171ea85e644c849f2c449c58d225d7
Quelldatensatz
uspto-grants-1998_10
Patentnummer
US05824333

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