Manganese/bipyridine-catalyzed non-directed C(sp3)–H bromination using NBS and TMSN3

A Mn(II)/bipyridine-catalyzed bromination reaction of unactivated aliphatic C(sp3)−H bonds has been developed using N-bromosuccinimide (NBS) as the brominating reagent. The reaction proceeded in moderate-to-good yield, even on a gram scale. The introduced bromine atom can be converted into fluorine and allyl groups.

Direct C-H halogenation is one of the most efficient methods used for the synthesis of halogenated organic molecules. This direct method involves the reaction of an alkane with Br 2 , CBr 4 , or H 2 O 2 -HBr under photolysis or at high temperatures in the absence of a catalyst (Scheme 1a) [14][15][16]. However, these reactions do not exhibit any selectivity due to the indiscriminate attack of bromine radicals on the C-H bonds in the substrate, which leads to the formation of a mixture of halogenated products. Electrophilic and radical C(sp 3 )−H halogenation at the benzylic and allylic position using N-halosuccinimide with azobisisobutyronitrile or benzoyl peroxide as a radical initiator is known as the Wohl-Ziegler bromination reaction, which requires heating, acidic/basic conditions, and/or UV irradiation (Scheme 1a) [17][18][19][20].
Herein, we report a manganese-catalyzed C(sp 3 )-H bromination reaction at the methine and benzylic positions of a wide range of substrates. The manganese catalyst, brominating agent, and additives are commercially available, and the reaction can be achieved by simply mixing these reagents with the substrate.

Results and Discussion
The reaction of isoamyl alcohol derivative 1a with N-bromosuccinimide (NBS) and TMSN 3 in the presence of a catalytic amount of Mn(OAc) 2 and bipyridine (bpy) in 1,2-dichloroethane (DCE) at 60 °C for 18 h gave C(sp 3 )-H brominated product 2a in 10% yield (Table 1, entry 1). Although the yield of 2a did not increase when performing the reaction in acetonitrile (Table 1, entry 2), the yield of 2a was dramatically improved to 62% using PhCF 3 as the solvent (Table 1, entry 3). Other manganese salts, such as MnBr 2 and Mn(acac) 2 , were also effective in the reaction, giving similar yields (Table 1, entries 4 and 5). Other first-row transition metal salts, such as Fe(OAc) 2 and Co(OAc) 2 , did not improve the yield of 2a (Table 1, entries 6 and 7). Product 2a was formed in 21 and 49% yields, respectively when the reaction was conducted in the absence of the transition metal salt and bpy ligand ( Table 1, entries 8 and 9). TMSN 3 was indispensable in this reaction because the C(sp 3 )-H bromination reaction did not occur in its absence (Table 1, entry 10). We then investigated the following experiments using the conditions described in entry 3.
Under the optimized reaction conditions, we investigated the C(sp 3 )-H bromination reaction of several substrates (Scheme 2). The reaction proceeded regioselectively at the methine C(sp 3 )-H bond of isoamyl benzoate (1b) to give 2b in 64% yield. Isoamyl benzoates bearing halogen atoms, such as fluorine, chlorine, or bromine, on the phenyl ring were also suitable substrates and gave C(sp 3 )-H brominated products 2c-e in 49-60% yields, without any loss of the halogen substituents.
Although the C(sp 3 )-H bromination of isobutyl benzoate 1f did not proceed at 60 °C, the corresponding C(sp 3 )-H brominated compound 2f was produced at higher temperature (80 °C). The C(sp 3 )-H bond in acetal 1g was efficiently brominated to give 2g in 79% yield. The reaction of adamantane (1h) proceeded selectively at the tertiary C(sp 3 )-H bond to give a mixture of mono-and dibrominated products (2h and 2h′). The selectivity of 2h and 2h′ can be controlled by varying the reaction time; mono-brominated 2h was obtained in 62% yield as the major product after 30 min of reaction and dibrominated 2h′ was afforded as the major product after 18 h. Similarly, 1,3dimethyladamantane (1i) and methyl adamantane-1-carboxylate (1j) were successfully converted to brominated products 2i and 2j, respectively. For benzeneacetic acid methyl esters 1k, 1l and 1m, the C(sp 3 )-H bromination reaction proceeded selectively at the benzylic position and their corresponding brominated products (2k, 2l and 2m) were obtained in 61, 57 and 55% yield, respectively.
We next investigated the regioselectivity of the reaction using substrates with two possible reaction sites. The reaction of substrate 1n bearing two methine C(sp 3 )-H bonds occurred selectively at the terminal position giving product 2n in 27% yield. The C(sp 3 )-H bromination reaction took place selectively at the methine C(sp 3 )-H bond when using substrate 1o, which has both methine and benzylic C(sp 3 )-H bonds, which gave product 2o in 30% yield.
The manganese-catalyzed C(sp 3 )-H bromination reaction proceeded in good yield, even on a gram scale. The reaction was performed using 2.61 g of 1a with NBS and TMSN 3 in the presence of a catalytic amount of Mn(OAc) 2 and bpy to give 1.98 g of 2a in 58% yield (Scheme 3).
The introduced bromine atom can be converted into other functional groups. The reaction of 2a with selectfluor in MeCN at 25 °C for 12 h gave fluorinated product 3 in 86% yield (Scheme 4, top) [50]. Allylated product 4 was obtained in 64% yield upon treating 2a with allyltributylstannane in the presence of a catalytic amount of AIBN (Scheme 4, bottom) [51].

Scheme 4:
Conversion of the C(sp 3 )-Br bond. Table 1 shows that the C(sp 3 )-H bromination reaction proceeds in the absence of a transition metal salt or bpy ligand, and was accelerated by transition metal salts, especially Mn(OAc) 2 . In addition, the results also suggest that TMSN 3 is required for the C(sp 3 )-H bromination reaction. The proposed reaction mechanism is shown in Scheme 5, which involves the following steps.
(1) The reaction between NBS and TMSN 3 generates bromine azide via the elimination of N-(trimethylsilyl)succinimide [52,53]; (2) bromine and azide radicals are then formed via homolytic cleavage of the weak Br-N 3 bond in bromine azide [54,55]; (3) the bromine radical can also be generated from NBS with the formation of a succinimide radical; (4) alkyl radical intermediate A is then formed via hydrogen abstraction by the succinimidyl radical and/or azidyl radical [56,57]; (5)

Conclusion
In summary, we have successfully developed a manganese-catalyzed bromination of unactivated aliphatic C(sp 3 )−H bonds. The reaction proceeded selectively at the methine and benzylic positions using simple and commercially available compounds, such as NBS, TMSN 3 , Mn(OAc) 2 , and bpy, even on a gram scale. Furthermore, the brominated products can be easily functionalized upon the introduction of other functional groups, Scheme 5: Proposed mechanism of manganese-catalyzed C(sp 3 )-H bromination.
such as fluorine and allyl groups. We hope that this C(sp 3 )-H bromination reaction will become a useful method to synthesize organic compounds with bromine atom(s).