3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid

Base Information

Chemical Name:3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid
CAS No.:300363-44-4
Molecular Formula:C₃₀H₃₇NO₅SSi
Molecular Weight:551.779
Hs Code.:

3-[[1-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid

Synonyms:3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid

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Chemical Property of 3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid

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Technology Process of 3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid

There total 4 articles about 3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid 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%

: 300363-43-3
3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid methyl ester

: 300363-44-4
3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid

Guidance literature:: With lithium hydroxide; In acetone;
DOI:10.1016/S0957-4166(00)00237-8

Reference yield:

: [(1R)-1-({[(1,1-dimethylethyl)(diphenyl)silyl]oxy}methyl)-2-propen-1-yl]amine

: 300363-44-4
3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / methanol

2: 98 percent / Et₃N / CH₂Cl₂ / 0 - 20 °C

3: 86 percent / aq. LiOH / acetone

With lithium hydroxide; triethylamine; In methanol; dichloromethane; acetone; 1: Michael addition / 2: Tosylation / 3: Hydrolysis;
DOI:10.1016/S0957-4166(00)00237-8

Reference yield:

: 300363-41-1
(+)-1,1-dimethylethyl [(1R)-1-({[(1,1-dimethylethyl)(diphenyl)silyl]oxy}methyl)prop-2-en-1-yl]carbamate

: 300363-44-4
3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / TBDMSTf; 2,6-lutidine / CH₂Cl₂ / 20 h / 20 °C

2: 94 percent / methanol

3: 98 percent / Et₃N / CH₂Cl₂ / 0 - 20 °C

4: 86 percent / aq. LiOH / acetone

With 2,6-dimethylpyridine; lithium hydroxide; t-butyldimethylsiyl triflate; triethylamine; In methanol; dichloromethane; acetone; 1: Ohfune deacylation / 2: Michael addition / 3: Tosylation / 4: Hydrolysis;
DOI:10.1016/S0957-4166(00)00237-8