“…Several attempts to synthesize C 6 (OFc) 6 failed, because of the low thermal stability of 1 compared with C 6 H 5 OH . Compound 6e is the second example of a molecule bearing five ether and one fluoro substituent …”
Abstract:The reaction of ferrocenol [FcOH; Fc = Fe(η 5 -C 5 H 5 )-(η 5 -C 5 H 4 )] with aryl fluorides ArH 6-n F n (n = 3-6) within a nucleophilic aromatic substitution reaction (S N Ar) gave ferrocenyloxysubstituted fluorobenzenes of general type C 6 H 0-3
“…Several attempts to synthesize C 6 (OFc) 6 failed, because of the low thermal stability of 1 compared with C 6 H 5 OH . Compound 6e is the second example of a molecule bearing five ether and one fluoro substituent …”
Abstract:The reaction of ferrocenol [FcOH; Fc = Fe(η 5 -C 5 H 5 )-(η 5 -C 5 H 4 )] with aryl fluorides ArH 6-n F n (n = 3-6) within a nucleophilic aromatic substitution reaction (S N Ar) gave ferrocenyloxysubstituted fluorobenzenes of general type C 6 H 0-3
“…Similar nucleophilic substitution of alkoxide anion equivalent 9 on an aromatic ring was achieved by the reaction of silyl ethers with hexafluorobenzene 7 in the presence of a catalytic amount of CsF as an initiator (Scheme 4) [4]. It was reported that the use of silyl ethers was more favorable for polyalkoxylation of 7 than alkali metal alkoxide.…”
“…When Me 3 SiCl/Et 3 N, was used, only a poor yield of the silylated product SCHEME 1 2a was formed, but in the case of hexamethyldisilazane with a catalytic amount of sodium saccharin [3], the silyl ethers 2a and 2b were formed in high yield irrespective of the fluoroalkyl chain length (Scheme 1).…”
Section: Resultsmentioning
confidence: 99%
“…The filtrate was dried in vacuo, giving 6a as very hygroscopic solid. 9,9,9,8,8,7,7,6,6,5,5,4,4- 3 P, 40%], 1.0 (s, 7A) and 1.7 (s, 7B, 60%). After 1 day: d ס 1.0 and 1.7 (60%), 114.0 (40%).…”
Section: General Procedures For Silylation Of Hydroxy Ketones 1abmentioning
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