(2S,4R)-tert-butyl 2-tert-butoxycarbonylamino-5-tert-butyldiphenylsilyloxy-4-methylpentanoate

Base Information

Chemical Name:(2S,4R)-tert-butyl 2-tert-butoxycarbonylamino-5-tert-butyldiphenylsilyloxy-4-methylpentanoate
CAS No.:913256-76-5
Molecular Formula:C₃₁H₄₇NO₅Si
Molecular Weight:541.803
Hs Code.:

Synonyms:(2S,4R)-tert-butyl 2-tert-butoxycarbonylamino-5-tert-butyldiphenylsilyloxy-4-methylpentanoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2S,4R)-tert-butyl 2-tert-butoxycarbonylamino-5-tert-butyldiphenylsilyloxy-4-methylpentanoate

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Technology Process of (2S,4R)-tert-butyl 2-tert-butoxycarbonylamino-5-tert-butyldiphenylsilyloxy-4-methylpentanoate

There total 8 articles about (2S,4R)-tert-butyl 2-tert-butoxycarbonylamino-5-tert-butyldiphenylsilyloxy-4-methylpentanoate 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: 75.0%

: 75-65-0
tert-butyl alcohol

: 913256-71-0
(6R,8S)-2,2,6,12,12-pentamethyl-10-oxo-3,3-diphenyl-4,11-dioxa-9-aza-3-silatridecane-8-carboxylic acid

: 913256-76-5
(2S,4R)-tert-butyl 2-tert-butoxycarbonylamino-5-tert-butyldiphenylsilyloxy-4-methylpentanoate

Guidance literature:: With dmap; di-tert-butyl dicarbonate; at 20 ℃; for 0.5h;
DOI:10.1002/ejoc.200600154

Reference yield:

: 92817-88-4
(2S)-3-{[tert-butyl(diphenyl)silyl]oxy}-2-methylpropanal

: 913256-76-5
(2S,4R)-tert-butyl 2-tert-butoxycarbonylamino-5-tert-butyldiphenylsilyloxy-4-methylpentanoate

Guidance literature:: Multi-step reaction with 6 steps

1.1: 70 percent / (i-Pr)2NEt; LiCl / acetonitrile / 24 h / 20 °C

2.1: 100 percent / H₂ / Pd/C / ethyl acetate / 18 h / 20 °C

3.1: KHMDS / tetrahydrofuran; toluene / 0.67 h / -80 °C

3.2: trisyl azide / tetrahydrofuran; toluene / 0.07 h / -80 °C

3.3: 68 percent / acetic acid / tetrahydrofuran; toluene / -80 - 20 °C

4.1: 99 percent / H₂ / Pd/C / ethyl acetate / 15 h / 20 °C

5.1: 92 percent / LiOH; aq. H₂O₂ / tetrahydrofuran; H₂O / 20 h / 24 °C

6.1: 75 percent / DMAP; Boc₂O / 0.5 h / 20 °C

With dmap; lithium hydroxide; di-tert-butyl dicarbonate; hydrogen; dihydrogen peroxide; potassium hexamethylsilazane; N-ethyl-N,N-diisopropylamine; lithium chloride; palladium on activated charcoal; In tetrahydrofuran; water; ethyl acetate; toluene; acetonitrile;
DOI:10.1002/ejoc.200600154

Reference yield:

: 95514-03-7
(S)-3-(tert-butyl-diphenyl-silanyloxy)-2-methyl-propionic acid methyl ester

: 913256-76-5
(2S,4R)-tert-butyl 2-tert-butoxycarbonylamino-5-tert-butyldiphenylsilyloxy-4-methylpentanoate

Guidance literature:: Multi-step reaction with 7 steps

1.1: 93 percent / DIBAL-H / toluene; diethyl ether / 1.25 h / -80 °C

2.1: 70 percent / (i-Pr)2NEt; LiCl / acetonitrile / 24 h / 20 °C

3.1: 100 percent / H₂ / Pd/C / ethyl acetate / 18 h / 20 °C

4.1: KHMDS / tetrahydrofuran; toluene / 0.67 h / -80 °C

4.2: trisyl azide / tetrahydrofuran; toluene / 0.07 h / -80 °C

4.3: 68 percent / acetic acid / tetrahydrofuran; toluene / -80 - 20 °C

5.1: 99 percent / H₂ / Pd/C / ethyl acetate / 15 h / 20 °C

6.1: 92 percent / LiOH; aq. H₂O₂ / tetrahydrofuran; H₂O / 20 h / 24 °C

7.1: 75 percent / DMAP; Boc₂O / 0.5 h / 20 °C

With dmap; lithium hydroxide; di-tert-butyl dicarbonate; hydrogen; dihydrogen peroxide; potassium hexamethylsilazane; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; lithium chloride; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; water; ethyl acetate; toluene; acetonitrile;
DOI:10.1002/ejoc.200600154