3-[(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy]-(2R)-propane-1,2-diol

Base Information

Chemical Name:3-[(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy]-(2R)-propane-1,2-diol
CAS No.:651031-10-6
Molecular Formula:C₂₇H₄₁NO₆Si
Molecular Weight:503.711
Hs Code.:

Synonyms:3-[(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy]-(2R)-propane-1,2-diol

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Chemical Property of 3-[(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy]-(2R)-propane-1,2-diol

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Technology Process of 3-[(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy]-(2R)-propane-1,2-diol

There total 5 articles about 3-[(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy]-(2R)-propane-1,2-diol 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: 86.0%

: 651031-09-3
(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy-(4S)-methyl-2,2-dimethyl-[1,3]-dioxolane

: 651031-10-6
3-[(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy]-(2R)-propane-1,2-diol

Guidance literature:: With acetic acid; at 20 ℃; for 24h;
DOI:10.1021/ol035998s

Reference yield:

: 2766-43-0
N-tert-butyloxycarbonyl-L-serine methyl ester

: 651031-10-6
3-[(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy]-(2R)-propane-1,2-diol

Guidance literature:: Multi-step reaction with 4 steps

1.1: 95 percent / imidazole / dimethylformamide / 2 h / 20 °C

2.1: 92 percent / LiBH₄ / diethyl ether / 0 - 20 °C

3.1: NaH / tetrahydrofuran / 0.25 h / cooling

3.2: 83 percent / tetrahydrofuran / 2.17 h

4.1: 86 percent / aq. AcOH / 24 h / 20 °C

With 1H-imidazole; lithium borohydride; sodium hydride; acetic acid; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1021/ol035998s

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 651031-10-6
3-[(2R)-2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propanoxy]-(2R)-propane-1,2-diol

Guidance literature:: Multi-step reaction with 4 steps

1.1: 95 percent / imidazole / dimethylformamide / 2 h / 20 °C

2.1: 92 percent / LiBH₄ / diethyl ether / 0 - 20 °C

3.1: NaH / tetrahydrofuran / 0.25 h / cooling

3.2: 83 percent / tetrahydrofuran / 2.17 h

4.1: 86 percent / aq. AcOH / 24 h / 20 °C

With 1H-imidazole; lithium borohydride; sodium hydride; acetic acid; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1021/ol035998s