(2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester

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Chemical Name:(2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester
CAS No.:135905-09-8
Molecular Formula:C₂₉H₅₃NO₉SSi₂
Molecular Weight:647.978
Hs Code.:

(2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester

Synonyms:(2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester

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Chemical Property of (2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester

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Technology Process of (2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester

There total 9 articles about (2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester 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: 90.0%

: 135905-10-1
(2SR,3SR,γSR)-1-(Benzyloxycarbonyl)-3-<2-(trimethylsilyl)ethoxymethoxy>-γ-<2-(trimethylsilyl)ethoxymethoxymethyl>pyrrolidine-2-propanol

: 124-63-0
methanesulfonyl chloride

: 135905-09-8
(2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 1h;

Reference yield:

: 76513-69-4
(2-trimethylethylsilylethoxy)methyl chloride

: 135905-09-8
(2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 78 percent / N,N-diisopropylethylamine / CH₂Cl₂ / 16 h / 40 °C

2: NaIO₄, OsO₄ / diethyl ether; H₂O / 16 h / Ambient temperature

3: 67 percent / NaBH₄ / ethanol / 0.5 h / 0 °C

4: 90 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

With sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; triethylamine; N-ethyl-N,N-diisopropylamine; In diethyl ether; ethanol; dichloromethane; water;

Reference yield:

: 95456-65-8,135970-35-3,136599-33-2,147511-83-9
(3aR,6aR)-2-Oxo-hexahydro-furo[3,2-b]pyrrole-4-carboxylic acid benzyl ester

: 135905-09-8
(2R,3R)-2-[(R)-3-Methanesulfonyloxy-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-propyl]-3-(2-trimethylsilanyl-ethoxymethoxy)-pyrrolidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 52 percent / LHMDS, HMPA / tetrahydrofuran; hexane / 1.) -78 deg C, 0.5 h, 2.) -78 deg C, 20 min; r.t., 1 h

2: 87 percent / NaBH₄ / ethanol / 0 °C

3: 78 percent / N,N-diisopropylethylamine / CH₂Cl₂ / 16 h / 40 °C

4: NaIO₄, OsO₄ / diethyl ether; H₂O / 16 h / Ambient temperature

5: 67 percent / NaBH₄ / ethanol / 0.5 h / 0 °C

6: 90 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; In tetrahydrofuran; diethyl ether; ethanol; hexane; dichloromethane; water;