(S,E)-1-benzyl-4-(benzyloxy)-5-(2-(tert-butyldiphenylsilyloxy)ethylidene)pyrrolidin-2-one

Base Information

Chemical Name:(S,E)-1-benzyl-4-(benzyloxy)-5-(2-(tert-butyldiphenylsilyloxy)ethylidene)pyrrolidin-2-one
CAS No.:1314768-39-2
Molecular Formula:C₃₆H₃₉NO₃Si
Molecular Weight:561.796
Hs Code.:

Synonyms:(S,E)-1-benzyl-4-(benzyloxy)-5-(2-(tert-butyldiphenylsilyloxy)ethylidene)pyrrolidin-2-one

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Chemical Property of (S,E)-1-benzyl-4-(benzyloxy)-5-(2-(tert-butyldiphenylsilyloxy)ethylidene)pyrrolidin-2-one

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Technology Process of (S,E)-1-benzyl-4-(benzyloxy)-5-(2-(tert-butyldiphenylsilyloxy)ethylidene)pyrrolidin-2-one

There total 3 articles about (S,E)-1-benzyl-4-(benzyloxy)-5-(2-(tert-butyldiphenylsilyloxy)ethylidene)pyrrolidin-2-one 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: 83.0%

: 1314768-36-9
(S,E)-1-benzyl-4-(benzyloxy)-5-(2-hydroxyethylidene)pyrrolidin-2-one

: 58479-61-1
tert-butylchlorodiphenylsilane

: 1314768-39-2
(S,E)-1-benzyl-4-(benzyloxy)-5-(2-(tert-butyldiphenylsilyloxy)ethylidene)pyrrolidin-2-one

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1080/00397911.2010.503003

Reference yield:

: 1314768-25-6
(S,E)-2-(1-benzyl-3-(benzyloxy)-5-oxopyrrolidin-2-ylidene)acetaldehyde

: 1314768-39-2
(S,E)-1-benzyl-4-(benzyloxy)-5-(2-(tert-butyldiphenylsilyloxy)ethylidene)pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate / methanol / 0.57 h / 0 °C / Inert atmosphere

2: dmap; triethylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With dmap; sodium tetrahydroborate; triethylamine; In methanol; dichloromethane;
DOI:10.1080/00397911.2010.503003

Reference yield:

: 1314768-35-8
(S)-1-benzyl-4-(benzyloxy)-5-ethynyl-5-hydroxy pyrrolidin-2-one

: 1314768-39-2
(S,E)-1-benzyl-4-(benzyloxy)-5-(2-(tert-butyldiphenylsilyloxy)ethylidene)pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: boron trifluoride diethyl etherate / dichloromethane / 0 °C / Inert atmosphere

2: sodium tetrahydroborate / methanol / 0.57 h / 0 °C / Inert atmosphere

3: dmap; triethylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With dmap; sodium tetrahydroborate; boron trifluoride diethyl etherate; triethylamine; In methanol; dichloromethane; 1: Meyer-Schuster rearrangement;
DOI:10.1080/00397911.2010.503003