nonyl-1-(tert-butyldimethylsilyloxymethyl)-(2R)-(4-methoxybenzyloxy)-(1R)-4-methylbenzenesulfonate

Base Information

Chemical Name:nonyl-1-(tert-butyldimethylsilyloxymethyl)-(2R)-(4-methoxybenzyloxy)-(1R)-4-methylbenzenesulfonate
CAS No.:463942-71-4
Molecular Formula:C₃₁H₅₀O₆SSi
Molecular Weight:578.886
Hs Code.:

Synonyms:nonyl-1-(tert-butyldimethylsilyloxymethyl)-(2R)-(4-methoxybenzyloxy)-(1R)-4-methylbenzenesulfonate

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Chemical Property of nonyl-1-(tert-butyldimethylsilyloxymethyl)-(2R)-(4-methoxybenzyloxy)-(1R)-4-methylbenzenesulfonate

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Technology Process of nonyl-1-(tert-butyldimethylsilyloxymethyl)-(2R)-(4-methoxybenzyloxy)-(1R)-4-methylbenzenesulfonate

There total 5 articles about nonyl-1-(tert-butyldimethylsilyloxymethyl)-(2R)-(4-methoxybenzyloxy)-(1R)-4-methylbenzenesulfonate 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: 80.0%

: 98-59-9
p-toluenesulfonyl chloride

: 463942-70-3
3-(4-methoxybenzyloxy)-1-tert-butyldimethylsilyloxy-(2S,3R)-decan-2-ol

: 463942-71-4
nonyl-1-(tert-butyldimethylsilyloxymethyl)-(2R)-(4-methoxybenzyloxy)-(1R)-4-methylbenzenesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 48h;
DOI:10.1016/S0040-4020(02)00423-4

Reference yield:

: 99745-00-3
(2S,3S)-2,3-epoxydecan-1-ol

: 463942-71-4
nonyl-1-(tert-butyldimethylsilyloxymethyl)-(2R)-(4-methoxybenzyloxy)-(1R)-4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / titanium(IV) isopropoxide / toluene / 2 h / Heating

2: 88 percent / imidazole / CH₂Cl₂ / 6 h / 20 °C

3: 80 percent / triethylamine / CH₂Cl₂ / 48 h / 20 °C

With 1H-imidazole; titanium(IV) isopropylate; triethylamine; In dichloromethane; toluene;
DOI:10.1016/S0040-4020(02)00423-4

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 463942-71-4
nonyl-1-(tert-butyldimethylsilyloxymethyl)-(2R)-(4-methoxybenzyloxy)-(1R)-4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / imidazole / CH₂Cl₂ / 6 h / 20 °C

2: 80 percent / triethylamine / CH₂Cl₂ / 48 h / 20 °C

With 1H-imidazole; triethylamine; In dichloromethane;
DOI:10.1016/S0040-4020(02)00423-4