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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 365239Erstellt: 24. Oktober 2026

Acetic Anhydride → Lactic Acid

https://huagongshe.com/de/reaction/365239

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt2-Hydroxyhexanoic acidHCID 99824—
EduktL-Lactic AcidHCID 107689—
LösungsmittelWaterHCID 962—
ProduktLactic AcidHCID 612—
Produkt2-Hydroxyhexanoic acidHCID 99824—

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

DL-2-Hydroxycaproic acid (1.00 gram, 0.0076 mole), and L-lactic acid (4.5 grams of a nominally 85% solution in water; 0.043 mole) were placed in a reaction flask equipped with a distillation head and mechanical stirrer. The flask was heated at 110° C. for 6 hours under low vacuum (aspirator) while water was removed. The temperature was then raised to 140° C. for 6 hours. Acetic anhydride (5.16 grams; 0.0506 moles) was added to the polymer, followed by heating at 80° C. for 14 hours. Excess acetic anhydride and acetic acid were distilled off under low vacuum. Tetrahydrofuran/water (15 mL of 85/15; volume/volume) was added with stirring and heating at 60° C. for 0.5 hour. The bulk of the solvent was removed by vacuum distillation on a rotary evaporator. The resulting crude product was dissolved in chloroform (20 mL). The chloroform solution was washed twice with millipore water (5 mL) and then dried with MgSO4. The mixture was filtered through a "d" fritted glass funnel and the solvent distilled from the polymer by rotary evaporation. Final traces of solvents were removed under high vacuum (0.4 mm Hg) on a Kugelrohr apparatus at 120° C. to provide acetyl-poly(DL-2-hydroxycaproic-co-L-lactic acid) with n=7.5 for lactic acid and 1.4 for hydroxycaproic acid, Mn=763, and Mw=1044 (by GPC).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06126919
Quelldatensatzuspto-grants-2000_10
ORD IDord-4927d39a35154dfa9d6b9525e9cbaaf9
Quellennotizuspto-grants-2000_10