((5E,7E,10E)-(S)-13-Hydroxy-2,8,10-trimethyl-trideca-5,7,10-trienyl)-(4-methoxy-benzyl)-carbamic acid 2-trimethylsilanyl-ethyl ester

Base Information

Chemical Name:((5E,7E,10E)-(S)-13-Hydroxy-2,8,10-trimethyl-trideca-5,7,10-trienyl)-(4-methoxy-benzyl)-carbamic acid 2-trimethylsilanyl-ethyl ester
CAS No.:213194-66-2
Molecular Formula:C₃₀H₄₉NO₄Si
Molecular Weight:515.809
Hs Code.:

Synonyms:((5E,7E,10E)-(S)-13-Hydroxy-2,8,10-trimethyl-trideca-5,7,10-trienyl)-(4-methoxy-benzyl)-carbamic acid 2-trimethylsilanyl-ethyl ester

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Chemical Property of ((5E,7E,10E)-(S)-13-Hydroxy-2,8,10-trimethyl-trideca-5,7,10-trienyl)-(4-methoxy-benzyl)-carbamic acid 2-trimethylsilanyl-ethyl ester

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Technology Process of ((5E,7E,10E)-(S)-13-Hydroxy-2,8,10-trimethyl-trideca-5,7,10-trienyl)-(4-methoxy-benzyl)-carbamic acid 2-trimethylsilanyl-ethyl ester

There total 14 articles about ((5E,7E,10E)-(S)-13-Hydroxy-2,8,10-trimethyl-trideca-5,7,10-trienyl)-(4-methoxy-benzyl)-carbamic acid 2-trimethylsilanyl-ethyl 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: 52.0%

: 213195-06-3
(3E,6E)-4,6-dimethyl-7-iodohepta-3,6-dien-1-ol

: 213195-28-9
D'

: 274-07-7
benzo[1,3,2]dioxaborole

: 213194-66-2
((5E,7E,10E)-(S)-13-Hydroxy-2,8,10-trimethyl-trideca-5,7,10-trienyl)-(4-methoxy-benzyl)-carbamic acid 2-trimethylsilanyl-ethyl ester

Guidance literature:: D'; benzo[1,3,2]dioxaborole; In tetrahydrofuran;

(3E,6E)-4,6-dimethyl-7-iodohepta-3,6-dien-1-ol; With sodium ethanolate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In ethanol; benzene; Heating;
DOI:10.7164/antibiotics.51.688

Reference yield:

: 13857-47-1
(E)-4-methylhept-3-en-6-yn-1-ol

: 213194-66-2
((5E,7E,10E)-(S)-13-Hydroxy-2,8,10-trimethyl-trideca-5,7,10-trienyl)-(4-methoxy-benzyl)-carbamic acid 2-trimethylsilanyl-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 99 percent / dimethylformamide

2.1: 88 percent / I₂ / Cp₂ZrCl₂ / CH₂Cl₂

3.1: 99 percent / TBAF / tetrahydrofuran

4.1: tetrahydrofuran

4.2: 52 percent / NaOEt / Pd(PPh₃)4 / ethanol; benzene / Heating

With tetrabutyl ammonium fluoride; iodine; zirconocene dichloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1.1: Etherification / 2.1: Addition / 3.1: Hydrolysis / 4.1: Addition / 4.2: Addition;
DOI:10.7164/antibiotics.51.688

Reference yield:

: 13927-59-8
(E)-7-acetoxy-4-methylhept-4-en-1-yne

: 213194-66-2
((5E,7E,10E)-(S)-13-Hydroxy-2,8,10-trimethyl-trideca-5,7,10-trienyl)-(4-methoxy-benzyl)-carbamic acid 2-trimethylsilanyl-ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 98 percent / KCN / ethanol

2.1: 99 percent / dimethylformamide

3.1: 88 percent / I₂ / Cp₂ZrCl₂ / CH₂Cl₂

4.1: 99 percent / TBAF / tetrahydrofuran

5.1: tetrahydrofuran

5.2: 52 percent / NaOEt / Pd(PPh₃)4 / ethanol; benzene / Heating

With potassium cyanide; tetrabutyl ammonium fluoride; iodine; zirconocene dichloride; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; 1.1: Deacetylation / 2.1: Etherification / 3.1: Addition / 4.1: Hydrolysis / 5.1: Addition / 5.2: Addition;
DOI:10.7164/antibiotics.51.688