Zobrazeno 1 - 3
of 3
pro vyhledávání: '"R. F. Fuller"'
Publikováno v:
Journal of Applied Chemistry. 3:266-274
Aryloxymethanesulphonic acids, ArO·CH2·SO3H, or their salts react readily at room temperature with chlorinating agents such as phosphorus pentachloride or thionyl chloride. Sulphur dioxide is eliminated and the hitherto unknown aryloxymethyl chlori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6098f66561360bfd70dec9dcdc323b36
https://doi.org/10.1002/jctb.5010030605
https://doi.org/10.1002/jctb.5010030605
Publikováno v:
Journal of Applied Chemistry. 3:409-416
Chloroanisoles (chlorine substituted in the nucleus) are chlorinated wholly in the side-chain at 190–200° in the presence of 1/20 molar proportion of phosphorus pentachloride. The three hydrogen atoms of the methoxy group are successively replaced
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccfa2b996bd1c646f034b25cd3bf82fd
https://doi.org/10.1002/jctb.5010030903
https://doi.org/10.1002/jctb.5010030903
Publikováno v:
Journal of Applied Chemistry. 3:253-258
Sodium aryloxymethanesulphonates are formed in good yield when a mixture of equimolecular proportions of sodium chloromethanesulphonate, a phenol and sodium hydroxide is heated for four hours at 200–220°. The reaction is a general one and has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e60961e4ca37eb41b2cd0968736a79bf
https://doi.org/10.1002/jctb.5010030603
https://doi.org/10.1002/jctb.5010030603