With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.209256-42-8,2,3-Dihydrobenzofuran-4-carbaldehyde,as a common compound, the synthetic route is as follows.
209256-42-8, 2,3-dihydrobenzofuran-4-carbaldehyde (2.00 g, 13.5 mmol) was dissolved in dry MeOH (30 mL) and the solution cooled to 0 C. NaBH4 (510 mg, 13.5 mmol) was added and the solution stirred at room temperature for 1 hour. Ice water was added and the layers separated. The organicphase was evaporated in vacuo to yield the title compound as colourless crystalline solid (1.90 g, 94%).[00292] AnalpH2_MeOH_4MIN: Rt: 2.00 mm, mlz 151.3 [M+H]+
As the paragraph descriping shows that 209256-42-8 is playing an increasingly important role.
Reference£º
Patent; UNIVERSITY OF LEEDS; PHILIPPOU, Helen; FOSTER, Richard; FISHWICK, Colin; REVILL, Charlotte; YULE, Ian; TAYLOR, Roger; NAYLOR, Alan; FALLON, Philip, Spencer; CROSBY, Stuart; HOPKINS, Anna; GUETZOYAN, Lucie, Juliette; MACNAIR, Alistair, James; STEWART, Mark, Richard; WINFIELD, Natalie, Louise; (273 pag.)WO2019/186164; (2019); A1;,
Benzofuran – Wikipedia
Benzofuran | C8H6O – PubChem