(S)-(+)-N-tert-butyloxycarbonyl-5-(triisopropylsilyloxymethyl)-3-phenylselenyl-pyrrolidin-2-one

Base Information

Chemical Name:(S)-(+)-N-tert-butyloxycarbonyl-5-(triisopropylsilyloxymethyl)-3-phenylselenyl-pyrrolidin-2-one
CAS No.:222307-20-2
Molecular Formula:C₂₅H₄₁NO₄SeSi
Molecular Weight:526.65
Hs Code.:

Synonyms:(S)-(+)-N-tert-butyloxycarbonyl-5-(triisopropylsilyloxymethyl)-3-phenylselenyl-pyrrolidin-2-one

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Chemical Property of (S)-(+)-N-tert-butyloxycarbonyl-5-(triisopropylsilyloxymethyl)-3-phenylselenyl-pyrrolidin-2-one

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Technology Process of (S)-(+)-N-tert-butyloxycarbonyl-5-(triisopropylsilyloxymethyl)-3-phenylselenyl-pyrrolidin-2-one

There total 5 articles about (S)-(+)-N-tert-butyloxycarbonyl-5-(triisopropylsilyloxymethyl)-3-phenylselenyl-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:

: 17342-08-4
(S)-Pyroglutaminol

: 222307-20-2
(S)-(+)-N-tert-butyloxycarbonyl-5-(triisopropylsilyloxymethyl)-3-phenylselenyl-pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 42.64 g / imidazole / CH₂Cl₂

2: 99 percent / 4-dimethylaminopyridine / acetonitrile / -30 - 20 °C

3: 1.) lithium bis(trimethylsilyl)amide / 1.) THF, 1 h, 2.) THF, overnight

With 1H-imidazole; dmap; lithium hexamethyldisilazane; In dichloromethane; acetonitrile;
DOI:10.1016/S0040-4020(98)01094-1

Reference yield:

: 13154-24-0
triisopropylsilyl chloride

: 222307-20-2
(S)-(+)-N-tert-butyloxycarbonyl-5-(triisopropylsilyloxymethyl)-3-phenylselenyl-pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 42.64 g / imidazole / CH₂Cl₂

2: 99 percent / 4-dimethylaminopyridine / acetonitrile / -30 - 20 °C

3: 1.) lithium bis(trimethylsilyl)amide / 1.) THF, 1 h, 2.) THF, overnight

With 1H-imidazole; dmap; lithium hexamethyldisilazane; In dichloromethane; acetonitrile;
DOI:10.1016/S0040-4020(98)01094-1

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 222307-20-2
(S)-(+)-N-tert-butyloxycarbonyl-5-(triisopropylsilyloxymethyl)-3-phenylselenyl-pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / 4-dimethylaminopyridine / acetonitrile / -30 - 20 °C

2: 1.) lithium bis(trimethylsilyl)amide / 1.) THF, 1 h, 2.) THF, overnight

With dmap; lithium hexamethyldisilazane; In acetonitrile;
DOI:10.1016/S0040-4020(98)01094-1