2-[2,3-dimethyl-4-(2-methylene-1-oxobutyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Base Information

Chemical Name:2-[2,3-dimethyl-4-(2-methylene-1-oxobutyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole
CAS No.:1370243-76-7
Molecular Formula:C₂₇H₂₅NO₂S
Molecular Weight:427.567
Hs Code.:

Synonyms:2-[2,3-dimethyl-4-(2-methylene-1-oxobutyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

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Chemical Property of 2-[2,3-dimethyl-4-(2-methylene-1-oxobutyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

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Technology Process of 2-[2,3-dimethyl-4-(2-methylene-1-oxobutyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

There total 9 articles about 2-[2,3-dimethyl-4-(2-methylene-1-oxobutyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: C₂₉H₃₂N₂O₂S

: 1370243-76-7
2-[2,3-dimethyl-4-(2-methylene-1-oxobutyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Guidance literature:: With sodium hydrogencarbonate; In water; at 85 ℃; for 0.666667h;
DOI:10.1016/j.bmc.2012.02.011

Reference yield:

: 1370244-44-2
2-[2,3-dimethyl-4-(1-oxo-butyl)phenoxy]ethanethioamide

: 1370243-76-7
2-[2,3-dimethyl-4-(2-methylene-1-oxobutyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Guidance literature:: Multi-step reaction with 3 steps

1: methanol / 24 h / Reflux

2: acetic acid / 1.5 h / 100 °C

3: sodium hydrogencarbonate / water / 0.67 h / 85 °C

With sodium hydrogencarbonate; acetic acid; In methanol; water; 2: Mannich reaction;
DOI:10.1016/j.bmc.2012.02.011

Reference yield:

: 35368-58-2
2-(2,3-dimethylphenoxy)acetamide

: 1370243-76-7
2-[2,3-dimethyl-4-(2-methylene-1-oxobutyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Guidance literature:: Multi-step reaction with 5 steps

1: tetraphosphorus decasulfide / tetrahydrofuran / 1.5 h / 50 °C

2: aluminum (III) chloride / carbon disulfide / 4.5 h / 20 - 50 °C

3: methanol / 24 h / Reflux

4: acetic acid / 1.5 h / 100 °C

5: sodium hydrogencarbonate / water / 0.67 h / 85 °C

With aluminum (III) chloride; tetraphosphorus decasulfide; sodium hydrogencarbonate; acetic acid; In tetrahydrofuran; methanol; carbon disulfide; water; 2: Friedel-Crafts acylation / 4: Mannich reaction;
DOI:10.1016/j.bmc.2012.02.011