Green synthesis of isoamyl acetate in glycerol triacetate

Adi Wolfson; Dina Saidkarimov; Christina Dlugy; Dorith Tavor

doi:10.1080/17518250903170850

Green synthesis of isoamyl acetate in glycerol triacetate

Adi Wolfson, Dina Saidkarimov, Christina Dlugy, Dorith Tavor

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

Abstract

Glycerol triacetate was successfully used as a green solvent and as the acyl donor in the production of isoamyl acetate by the transesterification of isoamyl alcohol over an acidic ion-exchange resin. Using glycerol triacetate as the solvent also enabled simple product recovery, easy catalyst separation and recycling, and microwave-promoted heating.

Original language	English
Pages (from-to)	107-110
Number of pages	4
Journal	Green Chemistry Letters and Reviews
Volume	2
Issue number	2
DOIs	https://doi.org/10.1080/17518250903170850
State	Published - 1 Dec 2009
Externally published	Yes

Keywords

Catalyst
Glycerol triacetate
Isoamyl acetate
Solid acid

ASJC Scopus subject areas

General Chemistry
Environmental Chemistry

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10.1080/17518250903170850

Cite this

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title = "Green synthesis of isoamyl acetate in glycerol triacetate",

abstract = "Glycerol triacetate was successfully used as a green solvent and as the acyl donor in the production of isoamyl acetate by the transesterification of isoamyl alcohol over an acidic ion-exchange resin. Using glycerol triacetate as the solvent also enabled simple product recovery, easy catalyst separation and recycling, and microwave-promoted heating.",

keywords = "Catalyst, Glycerol triacetate, Isoamyl acetate, Solid acid",

author = "Adi Wolfson and Dina Saidkarimov and Christina Dlugy and Dorith Tavor",

year = "2009",

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doi = "10.1080/17518250903170850",

language = "English",

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AU - Wolfson, Adi

AU - Saidkarimov, Dina

AU - Dlugy, Christina

AU - Tavor, Dorith

PY - 2009/12/1

Y1 - 2009/12/1

N2 - Glycerol triacetate was successfully used as a green solvent and as the acyl donor in the production of isoamyl acetate by the transesterification of isoamyl alcohol over an acidic ion-exchange resin. Using glycerol triacetate as the solvent also enabled simple product recovery, easy catalyst separation and recycling, and microwave-promoted heating.

AB - Glycerol triacetate was successfully used as a green solvent and as the acyl donor in the production of isoamyl acetate by the transesterification of isoamyl alcohol over an acidic ion-exchange resin. Using glycerol triacetate as the solvent also enabled simple product recovery, easy catalyst separation and recycling, and microwave-promoted heating.

KW - Catalyst

KW - Glycerol triacetate

KW - Isoamyl acetate

KW - Solid acid

UR - https://www.scopus.com/pages/publications/77951743423

U2 - 10.1080/17518250903170850

DO - 10.1080/17518250903170850

M3 - Article

AN - SCOPUS:77951743423

SN - 1751-8253

VL - 2

SP - 107

EP - 110

JO - Green Chemistry Letters and Reviews

JF - Green Chemistry Letters and Reviews

IS - 2

ER -

Green synthesis of isoamyl acetate in glycerol triacetate

Abstract

Keywords

ASJC Scopus subject areas

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