(4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-fluoromethylpyrrolidin-2-one

Base Information

Chemical Name:(4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-fluoromethylpyrrolidin-2-one
CAS No.:691407-30-4
Molecular Formula:C₂₇H₃₆FNO₄Si
Molecular Weight:485.671
Hs Code.:

Synonyms:(4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-fluoromethylpyrrolidin-2-one

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Chemical Property of (4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-fluoromethylpyrrolidin-2-one

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Technology Process of (4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-fluoromethylpyrrolidin-2-one

There total 4 articles about (4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-fluoromethylpyrrolidin-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: 61.0%

: 691407-27-9
(4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-hydroxymethylpyrrolidin-2-one

: 691407-30-4
(4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-fluoromethylpyrrolidin-2-one

Guidance literature:: With diethylamino-sulfur trifluoride; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1039/b316219b

Reference yield:

: 138871-58-6
(S)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-oxo-2,5-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

: 691407-30-4
(4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-fluoromethylpyrrolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / benzophenone / 24 h / 20 °C / Irradiation

2: 61 percent / Et₂NSF₃ / CH₂Cl₂ / 2 h / 20 °C

With benzophenone; diethylamino-sulfur trifluoride; In dichloromethane;
DOI:10.1039/b316219b

Reference yield:

: 691407-26-8
(4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-2-oxopyrrolidine-4-carbaldehyde

: 691407-30-4
(4S,5S)-N-tert-butoxycarbonyl-5-tert-butyldiphenylsilyloxymethyl-4-fluoromethylpyrrolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / NaBH₄ / methanol / 0.42 h / 20 °C

2: 61 percent / Et₂NSF₃ / CH₂Cl₂ / 2 h / 20 °C

With sodium tetrahydroborate; diethylamino-sulfur trifluoride; In methanol; dichloromethane;
DOI:10.1039/b316219b