tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate

Base Information

Chemical Name:tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate
CAS No.:1613450-12-6
Molecular Formula:C₂₁H₂₄FNO₅S
Molecular Weight:421.49
Hs Code.:

Synonyms:tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate

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Chemical Property of tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate

Chemical Property:

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Technology Process of tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate

There total 9 articles about tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate 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:

: 1613450-09-1
tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2-oxo-1,2,3-oxathiazolidine-4-carboxylate

: 1613450-12-6
tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate

Guidance literature:: With sodium periodate; rhodium(III) chloride hydrate; In water; acetonitrile; at 0 - 20 ℃; for 4.25h;
DOI:10.1016/j.tet.2014.05.004

Reference yield:

: 1613450-06-8
tert-butyl 2-(benzylamino)-2-(4-fluorobenzyl)-3-hydroxypropanoate

: 1613450-12-6
tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-imidazole; triethylamine; thionyl chloride / dichloromethane / 2.5 h / -10 - 20 °C / Inert atmosphere

2: rhodium(III) chloride hydrate; sodium periodate / water; acetonitrile / 4.25 h / 0 - 20 °C

With 1H-imidazole; sodium periodate; thionyl chloride; rhodium(III) chloride hydrate; triethylamine; In dichloromethane; water; acetonitrile;
DOI:10.1016/j.tet.2014.05.004

Reference yield:

: 55044-06-9,78715-83-0,103365-58-8,105308-52-9
methyl 2-phenyl-2-oxazoline-4-carboxylate

: 1613450-12-6
tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: sodium hydroxide / water; methanol; acetone / 3.33 h / 2 °C / Cooling with ice

2: hydrogenchloride / water / 1 h / 0 °C / pH < 3

3: dmap / dichloromethane; tert-butyl alcohol / 1 h / Inert atmosphere; Reflux

4: tetrabutylammomium bromide; potassium hydroxide / dichloromethane; toluene / 0 - 20 °C / Inert atmosphere

5: sodium cyanoborohydride / acetic acid / 16 h / 0 - 20 °C

6: 1H-imidazole; triethylamine; thionyl chloride / dichloromethane / 2.5 h / -10 - 20 °C / Inert atmosphere

7: rhodium(III) chloride hydrate; sodium periodate / water; acetonitrile / 4.25 h / 0 - 20 °C

With 1H-imidazole; hydrogenchloride; dmap; sodium periodate; thionyl chloride; rhodium(III) chloride hydrate; tetrabutylammomium bromide; sodium cyanoborohydride; triethylamine; potassium hydroxide; sodium hydroxide; In methanol; dichloromethane; water; acetic acid; acetone; toluene; acetonitrile; tert-butyl alcohol;
DOI:10.1016/j.tet.2014.05.004