N-{(1S,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(E)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide

Base Information

Chemical Name:N-{(1S,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(E)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide
CAS No.:211570-35-3
Molecular Formula:C₂₉H₃₈Cl₃NO₅Si
Molecular Weight:615.069
Hs Code.:

Synonyms:N-{(1S,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(E)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide

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Chemical Property of N-{(1S,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(E)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide

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Technology Process of N-{(1S,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(E)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide

There total 7 articles about N-{(1S,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(E)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide 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: 84.0%

: 211518-43-3
N-{(1R,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(R)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-phenylselanyl-ethyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide

: 211570-35-3
N-{(1S,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(E)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide

Guidance literature:: With dihydrogen peroxide; In tetrahydrofuran; water; at 0 - 20 ℃;
DOI:10.1039/a802741b

Reference yield:

: 114884-40-1
(S)-3,4-O-isopropylidene-3,4-dihydroxybutyltriphenylphosphonium iodide

: 211570-35-3
N-{(1S,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(E)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide

Guidance literature:: Multi-step reaction with 6 steps

2: 86 percent / PPTS / methanol / 0 °C

3: 92 percent / imidazole / dimethylformamide; CH₂Cl₂ / -60 °C

4: DBU / acetonitrile / 0 °C

5: 1.) methyl 2,2,2-trichloroacetimidate, Et₃N, 2.) PPTS / 1.) MeCN, -20 to -15 deg C, 2.) MeOH, H₂O, 20 deg C

6: 84 percent / H₂O₂ / H₂O; tetrahydrofuran / 0 - 20 °C

With 1H-imidazole; dihydrogen peroxide; pyridinium p-toluenesulfonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; methyl 2,2,2-trichloroacetimidate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1039/a802741b

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 211570-35-3
N-{(1S,2S)-4-(tert-Butyl-diphenyl-silanyloxy)-1-[(E)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-vinyl]-2-hydroxy-butyl}-2,2,2-trichloro-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / imidazole / dimethylformamide; CH₂Cl₂ / -60 °C

2: DBU / acetonitrile / 0 °C

3: 1.) methyl 2,2,2-trichloroacetimidate, Et₃N, 2.) PPTS / 1.) MeCN, -20 to -15 deg C, 2.) MeOH, H₂O, 20 deg C

4: 84 percent / H₂O₂ / H₂O; tetrahydrofuran / 0 - 20 °C

With 1H-imidazole; dihydrogen peroxide; pyridinium p-toluenesulfonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; methyl 2,2,2-trichloroacetimidate; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1039/a802741b