{(E)-(S)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-benzyl]-3-chlorosulfonyl-allyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{(E)-(S)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-benzyl]-3-chlorosulfonyl-allyl}-carbamic acid tert-butyl ester
CAS No.:210428-10-7
Molecular Formula:C₃₁H₃₈ClNO₅SSi
Molecular Weight:600.251
Hs Code.:

Synonyms:{(E)-(S)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-benzyl]-3-chlorosulfonyl-allyl}-carbamic acid tert-butyl ester

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Chemical Property of {(E)-(S)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-benzyl]-3-chlorosulfonyl-allyl}-carbamic acid tert-butyl ester

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Technology Process of {(E)-(S)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-benzyl]-3-chlorosulfonyl-allyl}-carbamic acid tert-butyl ester

There total 8 articles about {(E)-(S)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-benzyl]-3-chlorosulfonyl-allyl}-carbamic acid tert-butyl ester 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: 70.0%

: (E)-(S)-3-tert-Butoxycarbonylamino-4-[4-(tert-butyl-diphenyl-silanyloxy)-phenyl]-but-1-ene-1-sulfonatetetrabutyl-ammonium;

: 210428-10-7
{(E)-(S)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-benzyl]-3-chlorosulfonyl-allyl}-carbamic acid tert-butyl ester

Guidance literature:: With sulfuryl dichloride; 3 A molecular sieve; triphenylphosphine; In dichloromethane; for 3h; 0 to 25 deg C;

Reference yield:

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

: 210428-10-7
{(E)-(S)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-benzyl]-3-chlorosulfonyl-allyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 93 percent / NaHCO₃ / CH₂Cl₂ / 2 h / Ambient temperature

2: 89 percent / imidazole / CH₂Cl₂ / 4 h / Ambient temperature

3: 95 percent / DIBAL-H / toluene; tetrahydrofuran / -78 °C

4: 63 percent / nBuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C

5: acetone / Heating

6: 70 percent / SO₂Cl₂, Ph₃P, 3 Angstroem molecular sieves / CH₂Cl₂ / 3 h / 0 to 25 deg C

With 1H-imidazole; n-butyllithium; sulfuryl dichloride; 3 A molecular sieve; diisobutylaluminium hydride; sodium hydrogencarbonate; triphenylphosphine; In tetrahydrofuran; hexane; dichloromethane; acetone; toluene;

Reference yield:

: 4326-36-7
(S)-N-(tert-butoxycarbonyl)tyrosine methyl ester

: 210428-10-7
{(E)-(S)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-benzyl]-3-chlorosulfonyl-allyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 89 percent / imidazole / CH₂Cl₂ / 4 h / Ambient temperature

2: 95 percent / DIBAL-H / toluene; tetrahydrofuran / -78 °C

3: 63 percent / nBuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C

4: acetone / Heating

5: 70 percent / SO₂Cl₂, Ph₃P, 3 Angstroem molecular sieves / CH₂Cl₂ / 3 h / 0 to 25 deg C

With 1H-imidazole; n-butyllithium; sulfuryl dichloride; 3 A molecular sieve; diisobutylaluminium hydride; triphenylphosphine; In tetrahydrofuran; hexane; dichloromethane; acetone; toluene;