Synthetic Route of C8H11NO2. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: Methyl 2-(1-methyl-1H-pyrrol-2-yl)acetate, is researched, Molecular C8H11NO2, CAS is 51856-79-2, about Transition-Metal-Free Electrophilic Fluoroalkanesulfinylation of Electron-Rich (Het)Arenes with Fluoroalkyl Heteroaryl Sulfones via C(Het)-S and S=O Bond Cleavage. Author is Wei, Jun; Bao, Kun; Qi, Chengcheng; Liu, Yao; Ni, Chuanfa; Sheng, Rong; Hu, Jinbo.
A novel Ph2P(O)Cl-mediated direct fluoroalkanesulfinylation of electron-rich (het)arenes such as indole, 1-methyl-1H-pyrrole, 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline, etc. using fluoroalkyl heteroaryl sulfones I as the RnSO source (Rn = CF3, CF3(CF2)3, CF2Cl, CF2Br, CF2COOCH2CH3) was developed. This is the first example where 2-HetSO2Rf performs as the RfSO synthon in organic synthesis via both C(Het)-S and S = O bond cleavage.
In addition to the literature in the link below, there is a lot of literature about this compound(Methyl 2-(1-methyl-1H-pyrrol-2-yl)acetate)Synthetic Route of C8H11NO2, illustrating the importance and wide applicability of this compound(51856-79-2).
Reference:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem