acetic acid 5-(tert-butyl-dimethyl-silanyloxy)-5-[5-(tert-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl ester

Base Information

Chemical Name:acetic acid 5-(tert-butyl-dimethyl-silanyloxy)-5-[5-(tert-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl ester
CAS No.:409093-36-3
Molecular Formula:C₃₂H₅₁NO₆SSi₂
Molecular Weight:633.997
Hs Code.:

acetic acid 5-(<i>tert</i>-butyl-dimethyl-silanyloxy)-5-[5-(<i>tert</i>-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl ester

Synonyms:acetic acid 5-(tert-butyl-dimethyl-silanyloxy)-5-[5-(tert-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl ester

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Chemical Property of acetic acid 5-(tert-butyl-dimethyl-silanyloxy)-5-[5-(tert-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl ester

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Technology Process of acetic acid 5-(tert-butyl-dimethyl-silanyloxy)-5-[5-(tert-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl ester

There total 9 articles about acetic acid 5-(tert-butyl-dimethyl-silanyloxy)-5-[5-(tert-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl 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: 100.0%

: 64-19-7,77671-22-8
acetic acid

: 409093-42-1
N-{4-(tert-butyl-dimethyl-silanyloxy)-2-[1-(tert-butyl-dimethyl-silanyloxy)-5-hydroxy-pent-3-enyl]-phenyl}-4-methyl-benzenesulfonamide

: 409093-36-3
acetic acid 5-(tert-butyl-dimethyl-silanyloxy)-5-[5-(tert-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl ester

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at -20 ℃;
DOI:10.3987/COM-01-S(K)46

Reference yield:

: 394-31-0
2-amino-5-hydroxybenzoic acid

: 409093-36-3
acetic acid 5-(tert-butyl-dimethyl-silanyloxy)-5-[5-(tert-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: thionyl chloride

2: pyridine

3: imidazole

4: lithium borohydride

5: pyridinium dichromate / CH₂Cl₂

6: zinc; iodine / diethyl ether; benzene / Heating

7: 84 percent / imidazole

8: 80 percent / diisobutylaluminum hydride

9: 100 percent / dicyclohexylcarbodiimide; dimethylaminopyridine / CH₂Cl₂ / -20 °C

With pyridine; 1H-imidazole; dmap; dipyridinium dichromate; lithium borohydride; thionyl chloride; iodine; diisobutylaluminium hydride; dicyclohexyl-carbodiimide; zinc; In diethyl ether; dichloromethane; benzene; 6: Vinylogous Reformatsky reaction;
DOI:10.3987/COM-01-S(K)46

Reference yield:

: 1882-72-0
methyl 2-amino-5-hydroxybenzoate

: 409093-36-3
acetic acid 5-(tert-butyl-dimethyl-silanyloxy)-5-[5-(tert-butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonylamino)-phenyl]-pent-2-enyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: pyridine

2: imidazole

3: lithium borohydride

4: pyridinium dichromate / CH₂Cl₂

5: zinc; iodine / diethyl ether; benzene / Heating

6: 84 percent / imidazole

7: 80 percent / diisobutylaluminum hydride

8: 100 percent / dicyclohexylcarbodiimide; dimethylaminopyridine / CH₂Cl₂ / -20 °C

With pyridine; 1H-imidazole; dmap; dipyridinium dichromate; lithium borohydride; iodine; diisobutylaluminium hydride; dicyclohexyl-carbodiimide; zinc; In diethyl ether; dichloromethane; benzene; 5: Vinylogous Reformatsky reaction;
DOI:10.3987/COM-01-S(K)46