Brief introduction of C9H10O3

Name: 2,5-Dimethoxybenzaldehyde. Welcome to talk about 93-02-7, If you have any questions, you can contact Kumar, D; Prakasham, AP; Gangwar, MK; Ghosh, P or send Email.

Kumar, D; Prakasham, AP; Gangwar, MK; Ghosh, P in [Kumar, Dharmendra; Prakasham, A. P.; Gangwar, Manoj Kumar; Ghosh, Prasenjit] Indian Inst Technol, Dept Chem, Bombay 400076, Maharashtra, India published Solvent-free cyanosilylation of aromatic and heteroaryl aldehydes catalyzed by a cationic iron N-heterocyclic carbene complex at ambient temperature under UV irradiation in 2019.0, Cited 95.0. Name: 2,5-Dimethoxybenzaldehyde. The Name is 2,5-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 93-02-7.

The cyanosilylation of aromatic aldehydes and heteroaryl aldehydes with trimethylsilyl cyanide (TMSCN) is efficiently catalyzed by an iron complex of the type {[3-isopropyl-1-(1R-phenylethyl)imidazol-2-ylidene]Fe(CO)(2)}I (3) in presence of UV light (lambda = 294 nm) in moderate to excellent yields under ambient temperature. The heteroaryl aldehydes exhibited higher yields than the aromatic ones, and the aromatic aldehydes, bearing electron donating groups (EDG), exhibited higher yields over the ones with the electron withdrawing groups (EWG). A proposed catalytic cycle initiates with an active species (A), formed by the dissociation from the iron complex (3), and proceeds via an aldehyde activated species (B), and that upon reaction with TMSCN gives the desired cyanosilylated product. Quite significantly, the initial active iron species (A) and the iron-bound alpha-cyanobenzyloxy species (C) have been detected by mass spectrometry. Additionally, the formation of species (C) was further corroborated by the observation of the formation of TMSI in Si-29 NMR experiment.

Name: 2,5-Dimethoxybenzaldehyde. Welcome to talk about 93-02-7, If you have any questions, you can contact Kumar, D; Prakasham, AP; Gangwar, MK; Ghosh, P or send Email.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com