Research on new synthetic routes about Tris(2-(2-methoxyethoxy)ethyl)amine

The synthetic route of 70384-51-9 has been constantly updated, and we look forward to future research findings.

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 70384-51-9, name is Tris(2-(2-methoxyethoxy)ethyl)amine, A new synthetic method of this compound is introduced below., COA of Formula: C15H33NO6

EXAMPLE 61 8-(3,5-Bis-trifluoromethyl-benzoyl)-3-(6-chloro-pyrimidin-4-yl)-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one A mixture of 8-(3,5-bis-trifluoromethyl-benzoyl)-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one (0.1 g, 0.21 mmol), potassium carbonate (59 mg, 0.42 mmol), CuCl (2 mg, 0.021 mmol), tris[2-(2-methoxyethoxy)-ethyl]-amine (1.5 muL) and 4,6-dichloropyrimidine (32 mg, 0.21 mmol) in xylene (5 mL) was stirred and boiled for 18 h. The mixture was cooled, washed with water, ammonia in water (10percent) and water again. Evaporation of the solvent yielded a residue which was purified by chromatography on silica gel (ethyl acetate/n-hexane 1:2) to yield the desired product (29 mg, 24percent), m.p. 212-214° C. and MS: m/e=584.1 (M+H+).

The synthetic route of 70384-51-9 has been constantly updated, and we look forward to future research findings.

The important role of 70384-51-9

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route Tris(2-(2-methoxyethoxy)ethyl)amine, its application will become more common.

Reference of 70384-51-9,Some common heterocyclic compound, 70384-51-9, name is Tris(2-(2-methoxyethoxy)ethyl)amine, molecular formula is C15H33NO6, 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.

Synthesis of AMPS-ammonium salt monomer. A nitrogen purged 50 ml schlenk flask was charged with freshly distilled tris[2-(2-methoxyethoxy)-ethyl]amine (1.69 g, 5.24 mmol) and 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) (1.09 g, 5.24 mmol) and stirred at ambient temperature for 8 hr or until completely dissolved. Total dissolution completes formation of the AMPS-ammonium salt monomer as a transparent light amber oil in a 99percent yield which was used immediately without further purification.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route Tris(2-(2-methoxyethoxy)ethyl)amine, its application will become more common.

Reference:
Patent; The Government of the US, as represented by the Secretary of the Navy; US2008/51605; (2008); A1;,
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem