Continuously updated synthesis method about Ethyl 4-pyrazolecarboxylate

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route Ethyl 4-pyrazolecarboxylate, its application will become more common.

Synthetic Route of 37622-90-5,Some common heterocyclic compound, 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, molecular formula is C6H8N2O2, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

To a suspension of LAH (45.2 mL, 45.2 mmol, 1M in THF) in a flame-dried flask was added a solution of ethyl 1H-pyrazole-4-carboxylate (3.17 g, 22.6 mmol) in THF (20 mL) dropwise at 0 C. The reaction mixture was gradually warmed to rt and stirred overnight. The reaction mixture was cooled in an ice bath, and carefully quenched by sequential dropwise addition of 1.36 mL H2O, and 10 mL of 1M NaOH, followed by 20 min of stirring. Solid MgSO4 was added, the ice bath was removed, and stirring was continued for 30 min at rt. Solids were removed by filtration through Celite® and washed with THF, then MeOH. The combined filtrate was evaporated to give (1H- pyrazol-4-yl)methanol (1.75 g, 78.9percent), as a white solid.1H NMR (500MHz, DMSO-d6) delta 12.58 (br. s., 1H), 7.58 (s, 1H), 7.40 (s, 1H), 4.74 (t, J=5.5 Hz, 1H), 4.37 (d, J=5.2 Hz, 2H).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route Ethyl 4-pyrazolecarboxylate, its application will become more common.