Analyzing the synthesis route of 4265-25-2

As the paragraph descriping shows that 4265-25-2 is playing an increasingly important role.

4265-25-2, 2-Methylbenzofuran is a benzofuran compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated,4265-25-2

PREPARATION EXAMPLE 130 Tin tetrachloride (1.15 ml) was added to a solution of 6-bromohexanoyl chloride (2 g) and 2-methylbenzo[b]furan (1.24 g) in carbon disulfide (30 ml) under ice-cooling, the mixture was stirred at room temperature for 3 hr. Ice water and conc. hydrochloric acid were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, dried and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give 2.2 g of 6-bromo-1-(2-methyl-3-benzo[b]furyl)-1-hexanone. 1 H-NMR (CDCl3,ppm) delta: 1.52-1.63(2 H,m), 1.76-2.04(4 H,m), 2.78(3 H,s), 2.97(2 H,t,J=7.3 Hz), 3.44(2 H,t,J=6.6 Hz), 7.29-7.36(2 H,m), 7.42-7.47(1 H,m), 7.88-7.92(1 H,m)

As the paragraph descriping shows that 4265-25-2 is playing an increasingly important role.

Reference£º
Patent; Yoshitomi Pharmaceutical Industries, Ltd.; US5864039; (1999); A;,
Benzofuran – Wikipedia
Benzofuran | C8H6O – PubChem