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Process for preparing 2,2'-bis(diphenyl-phosphinylmethyl)-1,1'binaphtyl and novel compounds belonging to this group of substances

机译:制备2,2'-双(二苯基-膦基甲基)-1,1'联萘基的方法和属于该组物质的新化合物

摘要

Prodn. of 2,2'-bis(diphenylphosphinylmethyl)-1,1'-binaphthyls (I) comprises: (a) reacting 2,2'-dimethyl-1,1'-binaphthyl (II) with a brominating agent in a solvent to form 2,2'-bis(bromomethyl)-1,1'-binaphthyl (III) and other brominated binaphthyls; (b) opt. removing unreacted brominating agent, reacted brominating agent and/or solvent; and (c) reacting the prod. with an alkyl diphenylphosphinite of formula RO-P(Ar)2 (IV) at 70-180 degrees C, opt. in a solvent; where = R = 1-5C alkyl; and Ar = phenyl opt. mono- or disubstd. by 1-4C alkyl, CF3, F, Cl or Br. Also claimed are cpds. of formula (IA): Ar' = phenyl mono- or disubstd. by 1-4C alkyl, CF3, F, Cl or Br. Step (a) comprises reacting (II) with N-bromosuccinimide (NBS) in chlorobenzene and/or dichlorobenzene, either at -10 to +75 (esp. 0-40) degrees C in the presence of light with a wavelength of 10-10,000 nm, or at 25-150 (esp. 40-135) degrees C in the presence of a free radical source. Step (c) is effected at 100-170 (esp. 120-160) degrees C, opt. after replacing the (di)chlorobenzene with xylene and/or mesitylene.
机译:产品2,2'-双(二苯基膦基甲基)-1,1'-萘基(I)包括:(a)使2,2'-二甲基-1,1'-萘基(II)与溴化剂在溶剂中反应形式2,2'-双(溴甲基)-1,1'-联萘基(III)和其他溴化联萘基; (b)选择。除去未反应的溴化剂,反应的溴化剂和/或溶剂; (c)反应产物。选择在70-180摄氏度下使用式RO-P(Ar)2(IV)的烷基二苯基次膦酸酯。在溶剂中其中= R = 1-5C烷基; Ar =苯基。单或怀疑。 1-4C烷基,CF 3,F,Cl或Br。还声称有cpds。式(IA)的通式:Ar’=单或二苯基。 1-4C烷基,CF 3,F,Cl或Br。步骤(a)包括(II)与N-溴代琥珀酰亚胺(NBS)在氯苯和/或二氯苯中,在-10至+75(尤其是0-40)摄氏度,在波长为10- 10,000 nm,或在存在自由基源的情况下,在25-150(尤其是40-135)摄氏度的温度下。步骤(c)在100-170(尤其是120-160)摄氏度进行。用二甲苯和/或均三甲苯代替(二)氯苯后。

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