Share a compound : 85363-04-8

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, N-(tert-Butoxycarbonyl)-2-aminoacetonitrile, other downstream synthetic routes, hurry up and to see.

Adding a certain compound to certain chemical reactions, such as: 85363-04-8, name is N-(tert-Butoxycarbonyl)-2-aminoacetonitrile, belongs to nitriles-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 85363-04-8, Application In Synthesis of N-(tert-Butoxycarbonyl)-2-aminoacetonitrile

Boc-amino acetonitrile (1.00 g; 6.40 mmol) was dissolved in methanol (10 mL) and sodium methoxide (0.145 mL 25% in MeOH; 0.64 mmol) was added. The mixture was stirred at 20 C. for 18 hr, and subsequently ammonium chloride (0.34 g; 6.40 mmol) was added, and the mixture was stirred at 20 C. for 3 days. The solution was precipitated in diethyl ether (40 mL), and the precipitate was collected by filtration, washed, and dried to yield the amidine hydrochloride 17.

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, N-(tert-Butoxycarbonyl)-2-aminoacetonitrile, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; KONINKLIJKE PHILIPS N.V.; ROBILLARD, MARC STEFAN; JANSSEN, HENDRICUS MARIE; TEN HOEVE, WOLTER; VERSTEEGEN, RONNY MATHIEU; ROSSIN, RAFFAELLA; (131 pag.)US2016/106859; (2016); A1;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts