Literature DB >> 26629792

Halogen Exchange Reaction of Aliphatic Fluorine Compounds with Organic Halides as Halogen Source.

Yuki Mizukami1, Zhiyi Song1, Tamotsu Takahashi1.   

Abstract

The halogen exchange reaction of aliphatic fluorine compounds with organic halides as the halogen source was achieved. Treatment of alkyl fluorides (primary, secondary, or tertiary fluorides) with a catalytic amount of titanocene dihalides, trialkyl aluminum, and polyhalomethanes (chloro or bromo methanes) as the halogen source gave the corresponding alkyl halides in excellent yields under mild conditions. In the case of a fluorine/iodine exchange, no titanocene catalyst is needed. Only C-F bonds are selectively activated under these conditions, whereas alkyl chlorides, bromides, and iodides are tolerant to these reactions.

Entities:  

Year:  2015        PMID: 26629792     DOI: 10.1021/acs.orglett.5b02589

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Nickel-Catalyzed Cross-Electrophile Coupling of Aryl Chlorides with Primary Alkyl Chlorides.

Authors:  Seoyoung Kim; Matthew J Goldfogel; Michael M Gilbert; Daniel J Weix
Journal:  J Am Chem Soc       Date:  2020-05-21       Impact factor: 15.419

2.  Facile continuous process for gas phase halogen exchange over supported alkyl phosphonium salts.

Authors:  Priti Sharma; Yoel Sasson
Journal:  RSC Adv       Date:  2018-01-12       Impact factor: 3.361

3.  Selective synthesis of spirobiindanes, alkenyl chlorides, and monofluoroalkenes from unactivated gem-difluoroalkanes controlled by aluminum-based Lewis acids.

Authors:  Jiandong Wang; Yuta Ogawa; Norio Shibata
Journal:  Sci Rep       Date:  2019-12-13       Impact factor: 4.379

  3 in total

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