PROCESS FOR THE SELECTIVE SYNTHESIS OF SYLILALKYL DISULFIDES DESULFURATING THE CORRESPONDING POLYSULPHIDES WITH NUCLEOPHYLIC REAGENSES
Preparation of bis(silylalkyl)disulphanes of formula (R R R SiR )2S2 (I) comprises (1) reacting silylalkyl polysulphide(s) of formula (R R R SiR )2Sn (II) with a nucleophilic compound (III) of formula MCN (IIIA), M2SO3 (IIIB) or R R R P (IIIC) in an amount equimolar to the number of sulphur atoms to...
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| creator | JOERG MUENZENBERG THOMAS GOEBEL |
| description | Preparation of bis(silylalkyl)disulphanes of formula (R R R SiR )2S2 (I) comprises (1) reacting silylalkyl polysulphide(s) of formula (R R R SiR )2Sn (II) with a nucleophilic compound (III) of formula MCN (IIIA), M2SO3 (IIIB) or R R R P (IIIC) in an amount equimolar to the number of sulphur atoms to be removed from (II); (2) filtering the resultant solid; and (3) purifying (I). In the formulae, R -R , R -R = 1-8C alkyl and/or alkoxy, H or monovalent aryl, preferably phenyl, toluyl or benzyl; R = divalent 1-8C, preferably 2-4C alkylidene or a group of formula (IV); n = 3-20, preferably 3-10; and M = an alkali cation, optionally substituted ammonium ion or half alkaline earth or zinc ion. Preferably a mixture of (IIIA), (IIIB) and (IIIC) is used. Reaction is carried out in the presence of a solvent for (III) at a temperature between 20 degrees C and the b.pt. of the solvent, especially in a 2-phase system in the presence of a phase transfer catalyst. |
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In the formulae, R -R , R -R = 1-8C alkyl and/or alkoxy, H or monovalent aryl, preferably phenyl, toluyl or benzyl; R = divalent 1-8C, preferably 2-4C alkylidene or a group of formula (IV); n = 3-20, preferably 3-10; and M<+> = an alkali cation, optionally substituted ammonium ion or half alkaline earth or zinc ion. Preferably a mixture of (IIIA), (IIIB) and (IIIC) is used. Reaction is carried out in the presence of a solvent for (III) at a temperature between 20 degrees C and the b.pt. of the solvent, especially in a 2-phase system in the presence of a phase transfer catalyst.</description><edition>7</edition><language>eng</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2002</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20020430&DB=EPODOC&CC=HR&NR=P960516B1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20020430&DB=EPODOC&CC=HR&NR=P960516B1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JOERG MUENZENBERG</creatorcontrib><creatorcontrib>THOMAS GOEBEL</creatorcontrib><title>PROCESS FOR THE SELECTIVE SYNTHESIS OF SYLILALKYL DISULFIDES DESULFURATING THE CORRESPONDING POLYSULPHIDES WITH NUCLEOPHYLIC REAGENSES</title><description>Preparation of bis(silylalkyl)disulphanes of formula (R R R SiR )2S2 (I) comprises (1) reacting silylalkyl polysulphide(s) of formula (R R R SiR )2Sn (II) with a nucleophilic compound (III) of formula M<+>CN<-> (IIIA), M<+>2SO3<2-> (IIIB) or R R R P (IIIC) in an amount equimolar to the number of sulphur atoms to be removed from (II); (2) filtering the resultant solid; and (3) purifying (I). In the formulae, R -R , R -R = 1-8C alkyl and/or alkoxy, H or monovalent aryl, preferably phenyl, toluyl or benzyl; R = divalent 1-8C, preferably 2-4C alkylidene or a group of formula (IV); n = 3-20, preferably 3-10; and M<+> = an alkali cation, optionally substituted ammonium ion or half alkaline earth or zinc ion. Preferably a mixture of (IIIA), (IIIB) and (IIIC) is used. 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In the formulae, R -R , R -R = 1-8C alkyl and/or alkoxy, H or monovalent aryl, preferably phenyl, toluyl or benzyl; R = divalent 1-8C, preferably 2-4C alkylidene or a group of formula (IV); n = 3-20, preferably 3-10; and M<+> = an alkali cation, optionally substituted ammonium ion or half alkaline earth or zinc ion. Preferably a mixture of (IIIA), (IIIB) and (IIIC) is used. Reaction is carried out in the presence of a solvent for (III) at a temperature between 20 degrees C and the b.pt. of the solvent, especially in a 2-phase system in the presence of a phase transfer catalyst.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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| subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
| title | PROCESS FOR THE SELECTIVE SYNTHESIS OF SYLILALKYL DISULFIDES DESULFURATING THE CORRESPONDING POLYSULPHIDES WITH NUCLEOPHYLIC REAGENSES |
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