New learning discoveries about 104599-37-3

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 3,4-Dibromo-5-nitro-1H-pyrazole, other downstream synthetic routes, hurry up and to see.

Electric Literature of 104599-37-3, The chemical industry reduces the impact on the environment during synthesis 104599-37-3, name is 3,4-Dibromo-5-nitro-1H-pyrazole, I believe this compound will play a more active role in future production and life.

This intermediate, 3,4-dibromo-5-nitro-1H-pyrazole (69 g) was reduced by refluxing with Stannous chloride, dihydrate (135 g) in Ethyl acetate (600 mL) and Ethanol (300 mL) at 110 C. for 45 minutes. The yellow homogenous reaction solution was cooled to room temperature and slowly poured over a vigorously stirring solution of sodium bicarbonate (33 g) in water (200 mL) and ethyl acetate (800 mL). To the resultant slurry was added Celite (30 g), and this slurry was filtered through a bed of Celite. The filter cake was washed with additional ethyl acetate (600 mL). The organic solution was then washed with brine (200 mL), dried over sodium sulfate, filtered, and concentrated in vacuo to give the crude product as an orange oil. The crude product was then purified by flash column chromatography (Biotage, Quad 25; Eluent: 6% EtOH in methylene chloride). This afforded the title compound as a light beige solid (13.2 g, 32%). 1HNMR (400 MHz, DMSO-d6) delta: 5.20, (m, 3H), 11.60, (br s, 1H).

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 3,4-Dibromo-5-nitro-1H-pyrazole, other downstream synthetic routes, hurry up and to see.