(R)-2-{2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazol-4-yl}propan-1-ol

Base Information

Chemical Name:(R)-2-{2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazol-4-yl}propan-1-ol
CAS No.:693790-37-3
Molecular Formula:C₃₃H₄₁NO₄SSi
Molecular Weight:575.844
Hs Code.:

Synonyms:(R)-2-{2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazol-4-yl}propan-1-ol

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Chemical Property of (R)-2-{2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazol-4-yl}propan-1-ol

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Technology Process of (R)-2-{2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazol-4-yl}propan-1-ol

There total 9 articles about (R)-2-{2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazol-4-yl}propan-1-ol 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: 92.0%

: 693790-13-5
4-[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethyl]-2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazole

: 693790-37-3
(R)-2-{2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazol-4-yl}propan-1-ol

Guidance literature:: With acetic acid; In tetrahydrofuran; water; at 20 ℃; for 14h;
DOI:10.1139/v03-199

Reference yield:

: 693790-08-8
(S)-4-(tert-butyldiphenylsilanyloxy)-3-(4-methoxybenzyloxy)thiobutyramide

: 693790-37-3
(R)-2-{2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazol-4-yl}propan-1-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / 2,6-lutidine / CH₂Cl₂ / 14 h / 20 °C

2: 87 percent / (CF₃CO)2O; pyridine / CH₂Cl₂ / 0.33 h / -30 °C

3: 92 percent / AcOH / tetrahydrofuran; H₂O / 14 h / 20 °C

With pyridine; 2,6-dimethylpyridine; acetic acid; trifluoroacetic anhydride; In tetrahydrofuran; dichloromethane; water;
DOI:10.1139/v03-199

Reference yield:

: 693790-06-6
(S)-4-(tert-butyldiphenylsilanyloxy)-3-(4-methoxybenzyloxy)butyramide

: 693790-37-3
(R)-2-{2-[(S)-3-(tert-butyldiphenylsilanyloxy)-2-(4-methoxybenzyloxy)propyl]thiazol-4-yl}propan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / Lawesson's reagent / diisopropyl ether / 0.5 h / 20 °C

2: 73 percent / 2,6-lutidine / CH₂Cl₂ / 14 h / 20 °C

3: 87 percent / (CF₃CO)2O; pyridine / CH₂Cl₂ / 0.33 h / -30 °C

4: 92 percent / AcOH / tetrahydrofuran; H₂O / 14 h / 20 °C

With Lawessons reagent; pyridine; 2,6-dimethylpyridine; acetic acid; trifluoroacetic anhydride; In tetrahydrofuran; dichloromethane; di-isopropyl ether; water;
DOI:10.1139/v03-199