TY - JOUR
T1 - Convenient Unsymmetrical Disulfane Synthesis
T2 - Basic Zeolite-Catalyzed Thiol-Disulfane Exchange Reaction
AU - Yamamoto, Eiji
AU - Kawai, Yasutaka
AU - Takakura, Kei
AU - Kimura, Moemi
AU - Murayama, Haruno
AU - Matsueda, Hironobu
AU - Otsuki, Shujiro
AU - Sakata, Hiroshi
AU - Tokunaga, Makoto
N1 - Funding Information:
This work was financially supported by DIC corporation and Toyota Riken Scholar program.
Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2021/11/22
Y1 - 2021/11/22
N2 - Convenient catalytic synthetic methods for the preparation of unsymmetrical disulfanes are described. Na-exchanged X type zeolite (Na-X), commercially available as MS-13X, effectively catalyzes thiol-disulfane exchange reactions with 1.0 equivalent of thiols and 2.5–3.0 equivalents of disulfanes at 10 °C to room temperature under air. The reactions of sterically-hindered disulfanes or electron-deficient thiol substrates require high temperatures under inert atmospheres to maintain the good product yields. Various functionalized thiols and disulfanes are tolerant in the present catalytic systems, affording the corresponding unsymmetrical disulfanes in good-to-high yields (up to 96 %). The Na-X catalyst was successfully recycled 10 times without loss of yield. Preliminary mechanistic studies suggest the involvement of base-catalyzed SN2-S displacement and/or addition-elimination mechanisms, assisted by hydrogen-bonding interactions.
AB - Convenient catalytic synthetic methods for the preparation of unsymmetrical disulfanes are described. Na-exchanged X type zeolite (Na-X), commercially available as MS-13X, effectively catalyzes thiol-disulfane exchange reactions with 1.0 equivalent of thiols and 2.5–3.0 equivalents of disulfanes at 10 °C to room temperature under air. The reactions of sterically-hindered disulfanes or electron-deficient thiol substrates require high temperatures under inert atmospheres to maintain the good product yields. Various functionalized thiols and disulfanes are tolerant in the present catalytic systems, affording the corresponding unsymmetrical disulfanes in good-to-high yields (up to 96 %). The Na-X catalyst was successfully recycled 10 times without loss of yield. Preliminary mechanistic studies suggest the involvement of base-catalyzed SN2-S displacement and/or addition-elimination mechanisms, assisted by hydrogen-bonding interactions.
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U2 - 10.1002/cctc.202101092
DO - 10.1002/cctc.202101092
M3 - Article
AN - SCOPUS:85116730415
SN - 1867-3880
VL - 13
SP - 4694
EP - 4699
JO - ChemCatChem
JF - ChemCatChem
IS - 22
ER -