Isosorbide and dimethyl carbonate: a green match

In this review the reactivity of the bio-based platform compounds D-sorbitol and isosorbide with green reagents and solvent dimethyl carbonate (DMC) is reported. Dehydration of D-sorbitol via DMC in the presence of catalytic amounts of base is an efficient and viable process for the preparation of t...

Full description

Bibliographic Details
Main Authors: Fabio Aricò, Pietro Tundo
Format: Article
Language:English
Published: Beilstein-Institut 2016-10-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.12.218
_version_ 1818954576566419456
author Fabio Aricò
Pietro Tundo
author_facet Fabio Aricò
Pietro Tundo
author_sort Fabio Aricò
collection DOAJ
description In this review the reactivity of the bio-based platform compounds D-sorbitol and isosorbide with green reagents and solvent dimethyl carbonate (DMC) is reported. Dehydration of D-sorbitol via DMC in the presence of catalytic amounts of base is an efficient and viable process for the preparation of the industrially relevant anhydro sugar isosorbide. This procedure is “chlorine-free”, one-pot, environmental friendly and high yielding. The reactivity of isosorbide with DMC is equally interesting as it can lead to the formation of dicarboxymethyl isosorbide, a potential monomer for isosorbide-based polycarbonate, and dimethyl isosorbide, a high boiling green solvent. The peculiar reactivity of isosorbide and the non-toxic properties of DMC represent indeed a green match leading to several industrial appealing potential applications.
first_indexed 2024-12-20T10:24:22Z
format Article
id doaj.art-5c9fbdeb96644e828c08bebb4c8ac332
institution Directory Open Access Journal
issn 1860-5397
language English
last_indexed 2024-12-20T10:24:22Z
publishDate 2016-10-01
publisher Beilstein-Institut
record_format Article
series Beilstein Journal of Organic Chemistry
spelling doaj.art-5c9fbdeb96644e828c08bebb4c8ac3322022-12-21T19:43:51ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972016-10-011212256226610.3762/bjoc.12.2181860-5397-12-218Isosorbide and dimethyl carbonate: a green matchFabio Aricò0Pietro Tundo1Department of Environmental Sciences, Informatics and Statistics, Ca’ Foscari University, Scientific Campus Via Torino 155 , 30170 Venezia Mestre, ItalyDepartment of Environmental Sciences, Informatics and Statistics, Ca’ Foscari University, Scientific Campus Via Torino 155 , 30170 Venezia Mestre, ItalyIn this review the reactivity of the bio-based platform compounds D-sorbitol and isosorbide with green reagents and solvent dimethyl carbonate (DMC) is reported. Dehydration of D-sorbitol via DMC in the presence of catalytic amounts of base is an efficient and viable process for the preparation of the industrially relevant anhydro sugar isosorbide. This procedure is “chlorine-free”, one-pot, environmental friendly and high yielding. The reactivity of isosorbide with DMC is equally interesting as it can lead to the formation of dicarboxymethyl isosorbide, a potential monomer for isosorbide-based polycarbonate, and dimethyl isosorbide, a high boiling green solvent. The peculiar reactivity of isosorbide and the non-toxic properties of DMC represent indeed a green match leading to several industrial appealing potential applications.https://doi.org/10.3762/bjoc.12.218carbohydrate chemistryD-sorbitoldimethyl carbonategreen chemistryisosorbide
spellingShingle Fabio Aricò
Pietro Tundo
Isosorbide and dimethyl carbonate: a green match
Beilstein Journal of Organic Chemistry
carbohydrate chemistry
D-sorbitol
dimethyl carbonate
green chemistry
isosorbide
title Isosorbide and dimethyl carbonate: a green match
title_full Isosorbide and dimethyl carbonate: a green match
title_fullStr Isosorbide and dimethyl carbonate: a green match
title_full_unstemmed Isosorbide and dimethyl carbonate: a green match
title_short Isosorbide and dimethyl carbonate: a green match
title_sort isosorbide and dimethyl carbonate a green match
topic carbohydrate chemistry
D-sorbitol
dimethyl carbonate
green chemistry
isosorbide
url https://doi.org/10.3762/bjoc.12.218
work_keys_str_mv AT fabioarico isosorbideanddimethylcarbonateagreenmatch
AT pietrotundo isosorbideanddimethylcarbonateagreenmatch