(2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-carboxylate

Base Information

Chemical Name:(2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-carboxylate
CAS No.:1318129-49-5
Molecular Formula:C₄₁H₄₃NO₃Si
Molecular Weight:625.883
Hs Code.:

Synonyms:(2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-carboxylate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-carboxylate

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Technology Process of (2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-carboxylate

There total 1 articles about (2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-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: 100.0%

: 129430-93-9,129430-94-0
methyl (2S,4R)-4-hydroxy-1-tritylpyrrolidine-2-carboxylate

: 58479-61-1
tert-butylchlorodiphenylsilane

: 1318129-49-5
(2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-carboxylate

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1021/ol201769b

Reference yield: 52.0%

: 1318129-49-5
(2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-carboxylate

: 1318128-16-3
((2S,4R)-4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidin-2-yl)methanol

Guidance literature:: (2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-carboxylate; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 2.16667h;

With water; sodium hydroxide; In tetrahydrofuran; at 0 ℃;
DOI:10.1021/ol201769b

Reference yield:

: 1318129-49-5
(2S,4R)-methyl 4-(tert-butyldiphenylsilyloxy)-1-tritylpyrrolidine-2-carboxylate

: 1318128-51-6
(3R,5R)-3-azido-5-(tert-butyldiphenylsilyloxy)-1-tritylpiperidine

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 2.17 h / 0 - 20 °C

1.2: 0 °C

2.1: tetrabutylammoniun azide; ethanaminium,N-(difluoro-λ⁴-sulfanylidene)-N-ethyl-,tetrafluoroborate / dichloromethane / 0.5 h / 0 °C

With lithium aluminium tetrahydride; tetrabutylammoniun azide; ethanaminium,N-(difluoro-λ⁴-sulfanylidene)-N-ethyl-,tetrafluoroborate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ol201769b