Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the 'proton sponge coin'

被引:14
|
作者
Antonov, Alexander S. [1 ]
Pozharskii, Alexander F. [1 ]
Ozeryanskii, Valery A. [1 ]
Filarowski, Aleksander [2 ,3 ]
Suponitsky, Kyrill Yu. [4 ]
Tolstoy, Peter M. [5 ]
Vovk, Mikhail A. [5 ]
机构
[1] Southern Fed Univ, Dept Organ Chem, Rostov Na Donu 344090, Russia
[2] Univ Wroclaw, Fac Chem, PL-50383 Wroclaw, Poland
[3] Joint Inst Nucl Res, Frank Lab Neutron Phys, Dubna 141980, Russia
[4] Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 119991, Russia
[5] St Petersburg State Univ, Dept Chem, St Petersburg 198504, Russia
基金
俄罗斯基础研究基金会;
关键词
PERI-NAPHTHYLENEDIAMINES; HYDROGEN-BOND; SPECTROSCOPY; CONFORMERS; BASE;
D O I
10.1039/c5dt02482j
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
It has been found that 1,8- bis(dimethylamino) naphthalene (DMAN), unlike N,N-dimethylaniline, undergoes ring metallation in the n-BuLi-TMEDA-Et2O system with a low selectivity and in poor total yields. The situation is significantly improved in the t-BuLi- TMEDA-n-hexane system when 3- and 4-lithium derivatives become the only reaction products obtained in good yields. The formation of 3-Li-DMAN is especially desired since no method of direct meta-functionalization of DMAN is known to date. The relative stability and structure of DMAN lithium derivatives have been examined with the help of X-ray and multinuclear NMR measurements as well as DFT calculations.
引用
收藏
页码:17756 / 17766
页数:11
相关论文
共 50 条
  • [1] RADICAL ANION OF 1,8-BIS(DIMETHYLAMINO)NAPHTHALENE (PROTON SPONGE)
    GERSON, F
    HASELBAC.E
    PLATTNER, G
    CHEMICAL PHYSICS LETTERS, 1971, 12 (02) : 316 - &
  • [2] Inversion of states in two conformers of 1,8-bis(dimethylamino) naphthalene - the proton sponge
    Szemik-Hojniak, A
    Deperasinska, I
    Allonas, X
    Jacques, P
    JOURNAL OF MOLECULAR STRUCTURE, 2000, 526 : 219 - 225
  • [3] First transition metal complex of 1,8-bis(dimethylamino)naphthalene (proton sponge)
    Yamasaki, T
    Ozaki, N
    Saika, Y
    Ohta, K
    Goboh, K
    Nakamura, F
    Hashimoto, M
    Okeya, S
    CHEMISTRY LETTERS, 2004, 33 (07) : 928 - 929
  • [4] Charge density distribution in the "proton sponge" compound 1,8-bis(dimethylamino)naphthalene
    Mallinson, PR
    Wozniak, K
    Wilson, CC
    McCormack, KL
    Yufit, DS
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (19) : 4640 - 4646
  • [5] STRUCTURE AND IR-SPECTRA OF PROTONATED 1,8-BIS(DIMETHYLAMINO)NAPHTHALENE PROTON SPONGE
    BRZEZINSKI, B
    GLOWIAK, T
    GRECH, E
    MALARSKI, Z
    SOBCZYK, L
    CROATICA CHEMICA ACTA, 1992, 65 (01) : 101 - 108
  • [6] 1,8-BIS(DIMETHYLAMINOMETHYL)NAPHTHALENE - A NEW PROTON SPONGE
    BRZEZINSKI, B
    GLOWIAK, T
    GRECH, E
    MALARSKI, Z
    SOBCZYK, L
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1991, (10): : 1643 - 1647
  • [7] REMARKABLE BASICITY OF 1,8-BIS(DIMETHYLAMINO)NAPHTHALENE
    ALDER, RW
    BOWMAN, PS
    STEELE, WRS
    WINTERMAN, DR
    CHEMICAL COMMUNICATIONS, 1968, (13) : 723 - +
  • [8] 1,8-bis(hexamethyltriaminophosphazenyl)naphthalene, HMPN: A superbasic bisphosphazene "proton sponge"
    Raab, V
    Gauchenova, E
    Merkoulov, A
    Harms, K
    Sundermeyer, J
    Kovacevic, B
    Maksic, ZB
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (45) : 15738 - 15743
  • [9] AB-INITIO STUDIES OF PROTON SPONGES - 1,8-BIS(DIMETHYLAMINO)NAPHTHALENE
    PLATTS, JA
    HOWARD, ST
    WOZNIAK, K
    JOURNAL OF ORGANIC CHEMISTRY, 1994, 59 (16): : 4647 - 4651
  • [10] peri-naphthylenediamines25. Evidence for the participation of a radical cation of 1,8-bis(dimethylamino)naphthalene (“proton sponge”) in reactions with nitrating agents. The formation of 1,1′-binaphthyl “proton sponge” and the regioselective synthesis of 4-chloro-1,8-bis(dimethylamino)naphthalene
    V. A. Ozeryanskii
    A. F. Pozharskii
    A. M. Fomchenkov
    Russian Chemical Bulletin, 1998, 47 : 313 - 317