[(2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidin-2-yl]methanol

Base Information

Chemical Name:[(2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidin-2-yl]methanol
CAS No.:635299-81-9
Molecular Formula:C₁₈H₃₁NO₂Si
Molecular Weight:321.535
Hs Code.:

Synonyms:[(2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidin-2-yl]methanol

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Chemical Property of [(2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidin-2-yl]methanol

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Technology Process of [(2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidin-2-yl]methanol

There total 8 articles about [(2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidin-2-yl]methanol 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: 86.1%

: 1271809-99-4
methyl (2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidine-2-carboxylate

: 635299-81-9
[(2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidin-2-yl]methanol

Guidance literature:: With lithium borohydride; In tetrahydrofuran; at 0 - 30 ℃; for 16h; Inert atmosphere;

Reference yield:

: 114676-53-8
(2R,4R)-methyl 1-benzyl-4-hydroxypyrrolidine-2-carboxylate

: 635299-81-9
[(2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidin-2-yl]methanol

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dmap / dichloromethane / 24 h / 30 °C

2: lithium borohydride / tetrahydrofuran / 16.5 h / 0 - 30 °C

With lithium borohydride; triethylamine; dmap; In tetrahydrofuran; dichloromethane;

Reference yield:

: 2584-71-6,30724-02-8
cis-hydroxy-D-proline

: 635299-81-9
[(2R,4R)-1-benzyl-4-[tert-butyl(dimethyl)silyl]oxy-pyrrolidin-2-yl]methanol

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / 72 h / 0 - 20 °C

2: triethylamine / dichloromethane / 16 h / Reflux

3: triethylamine / dmap / dichloromethane / 24 h / 30 °C

4: lithium borohydride / tetrahydrofuran / 16.5 h / 0 - 30 °C

With lithium borohydride; thionyl chloride; triethylamine; dmap; In tetrahydrofuran; dichloromethane;