2013
DOI: 10.1155/2013/642479
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Efficient and Rapid Solvent‐Free Acetylation of Alcohols, Phenols, and Thiols Using Catalytic Amounts of Sodium Acetate Trihydrate

Abstract: Under solvent-free conditions, different alcohols and phenols were efficiently acetylated at room temperature within short time periods by using acetic anhydride in the presence of catalytic quantities of sodium acetate trihydrate, which is a very inexpensive and mild reagent. Thiols were also shown to behave equally well under the same conditions. Chemoselective protection of less hindered alcohols in the presence of bulkier homologues and phenols in the presence of alcohols was achieved using competitive exp… Show more

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Cited by 17 publications
(8 citation statements)
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“…Chrysanthemol was identified with an authentic standard (Sigma, Saint Louis, MO). The standard of chrysanthemyl acetate was prepared by acetylation of chrysanthemol as described (Mojtahedi and Samadian, ). The chrysanthemol emission from transgenic plants was quantified based on calibration curves with the authentic standard.…”
Section: Methodsmentioning
confidence: 99%
“…Chrysanthemol was identified with an authentic standard (Sigma, Saint Louis, MO). The standard of chrysanthemyl acetate was prepared by acetylation of chrysanthemol as described (Mojtahedi and Samadian, ). The chrysanthemol emission from transgenic plants was quantified based on calibration curves with the authentic standard.…”
Section: Methodsmentioning
confidence: 99%
“…The antimicrobial sustainability of samples coating on microscope slides was performed according to the literature. [44] The polymer coated glass surface were challenged with E.coli and S. aureus at a concentration of about and the plates were incubated for 24 h at 37 °C and counted for colonyforming units. In the study, 25 mm diameter empty glass material (NC) and solvent (DMSO) coated glass material (SC) used as control samples.…”
Section: Antibacterial Activitymentioning
confidence: 99%
“…On the other hand, some mixed reviews have been proposed for the reactivity of the hydroxyl group in cellulose that all hydroxyl groups participate and convert into cellulose acetate. [51][52][53][54][55]…”
Section: Gibbs Free Energy Calculationsmentioning
confidence: 99%