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Merck

Synthesis of cellulose methylcarbonate in ionic liquids using dimethylcarbonate.

ChemSusChem (2014-11-08)
Sara R Labafzadeh, K Juhani Helminen, Ilkka Kilpeläinen, Alistair W T King
RESUMO

Dialkylcarbonates are viewed as low-cost, low-toxicity reagents, finding application in many areas of green chemistry. Homogeneous alkoxycarbonylation of cellulose was accomplished by applying dialkycarbonates (dimethyl and diethyl carbonate) in the ionic liquid-electrolyte trioctylphosphonium acetate ([P8881 ][OAc])/DMSO or 1-ethyl-3-methylimidazolium acetate ([emim][OAc]). Cellulose dialkylcarbonates with a moderate degree of substitution (DS∼1) are accessible via this procedure and cellulose methylcarbonate was thoroughly characterized for its chemical and physical properties after regeneration. This included HSQC & HMBC NMR, ATR-IR, molecular weight distribution, morphology, thermal properties, and barrier properties after film formation.

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Sigma-Aldrich
Diethyl carbonate, anhydrous, ≥99%