(R)-(-)-[4-alcoxy-1-(2'-hydroxy-1'-phenyl-ethyl)-2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl]-dimethyl sulfonium

Base Information

Chemical Name:(R)-(-)-[4-alcoxy-1-(2'-hydroxy-1'-phenyl-ethyl)-2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl]-dimethyl sulfonium
CAS No.:1174637-73-0
Molecular Formula:C₁₅H₁₉NO₃S
Molecular Weight:293.387
Hs Code.:

Synonyms:(R)-(-)-[4-alcoxy-1-(2'-hydroxy-1'-phenyl-ethyl)-2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl]-dimethyl sulfonium

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Chemical Property of (R)-(-)-[4-alcoxy-1-(2'-hydroxy-1'-phenyl-ethyl)-2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl]-dimethyl sulfonium

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Technology Process of (R)-(-)-[4-alcoxy-1-(2'-hydroxy-1'-phenyl-ethyl)-2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl]-dimethyl sulfonium

There total 1 articles about (R)-(-)-[4-alcoxy-1-(2'-hydroxy-1'-phenyl-ethyl)-2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl]-dimethyl sulfonium 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: 87.0%

: 1174637-71-8
(R)-(-)-{[(2-hydroxy-1-phenyl-ethyl)-(2-methoxycarbonyl-ethyl)-carbamoyl]-methyl}-dimethyl-sulfonium bromide

: 1174637-73-0
(R)-(-)-[4-alcoxy-1-(2'-hydroxy-1'-phenyl-ethyl)-2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl]-dimethyl sulfonium

Guidance literature:: With potassium hydroxide; In acetonitrile; at 20 ℃; for 15h;
DOI:10.1016/j.tetlet.2009.02.143

Reference yield: 65.0%

: 1174637-73-0
(R)-(-)-[4-alcoxy-1-(2'-hydroxy-1'-phenyl-ethyl)-2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl]-dimethyl sulfonium

: 1174637-75-2
(R)-(-)-1-(2-hydroxy-1-phenyl-ethyl)-piperidine-2,4-dione

Guidance literature:: With hydrogenchloride; palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃; for 17h; Ultrasound activation;
DOI:10.1016/j.tetlet.2009.02.143