(2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-(pentyloxy)pyrrolidine-1-carboxylate

Base Information

Chemical Name:(2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-(pentyloxy)pyrrolidine-1-carboxylate
CAS No.:1610035-88-5
Molecular Formula:C₃₁H₄₇NO₄Si
Molecular Weight:525.804
Hs Code.:

Synonyms:(2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-(pentyloxy)pyrrolidine-1-carboxylate

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Chemical Property of (2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-(pentyloxy)pyrrolidine-1-carboxylate

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Technology Process of (2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-(pentyloxy)pyrrolidine-1-carboxylate

There total 4 articles about (2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-(pentyloxy)pyrrolidine-1-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: 69.0%

: 110-53-2
1-Bromopentane

: 1610035-87-4
(2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-hydroxypyrrolidine-1-carboxylate

: 1610035-88-5
(2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-(pentyloxy)pyrrolidine-1-carboxylate

Guidance literature:: With sodium hydride; In tetrahydrofuran; mineral oil; at 0 - 67 ℃; for 24h;

Reference yield:

: 135042-12-5,946610-68-0
(4R)-1-(tert-butoxycarbonyl)-4-hydroxy-D-proline

: 1610035-88-5
(2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-(pentyloxy)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 0.75 h / -10 °C

1.2: 2 h / 0 °C

2.1: 1H-imidazole; tert-butylchlorodiphenylsilane / N,N-dimethyl-formamide / 2 h / 20 °C

3.1: sodium hydride / tetrahydrofuran; mineral oil / 24 h / 0 - 67 °C

With 4-methyl-morpholine; 1H-imidazole; sodium hydride; tert-butylchlorodiphenylsilane; isobutyl chloroformate; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil;

Reference yield:

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

: 1610035-88-5
(2R,4R)-tert-butyl 2-(((tert-butyldiphenylsilyl)oxy)methyl)-4-(pentyloxy)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydroxide / tetrahydrofuran; water / 13 h / 25 °C

2.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 0.75 h / -10 °C

2.2: 2 h / 0 °C

3.1: 1H-imidazole; tert-butylchlorodiphenylsilane / N,N-dimethyl-formamide / 2 h / 20 °C

4.1: sodium hydride / tetrahydrofuran; mineral oil / 24 h / 0 - 67 °C

With 4-methyl-morpholine; 1H-imidazole; sodium hydride; tert-butylchlorodiphenylsilane; sodium hydroxide; isobutyl chloroformate; In tetrahydrofuran; water; N,N-dimethyl-formamide; mineral oil;