tert-Butyl-{(1S,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4-methyl-hept-6-enyloxy}-dimethyl-silane

Base Information

Chemical Name:tert-Butyl-{(1S,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4-methyl-hept-6-enyloxy}-dimethyl-silane
CAS No.:325172-43-8
Molecular Formula:C₂₆H₄₆O₅Si
Molecular Weight:466.734
Hs Code.:

Synonyms:tert-Butyl-{(1S,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4-methyl-hept-6-enyloxy}-dimethyl-silane

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Chemical Property of tert-Butyl-{(1S,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4-methyl-hept-6-enyloxy}-dimethyl-silane

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Technology Process of tert-Butyl-{(1S,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4-methyl-hept-6-enyloxy}-dimethyl-silane

There total 9 articles about tert-Butyl-{(1S,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4-methyl-hept-6-enyloxy}-dimethyl-silane 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: 90.0%

: 325172-42-7
toluene-4-sulfonic acid 2-[3-(tert-butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-1-methoxymethoxy-pentyl]-pent-4-enyl ester

: 325172-43-8
tert-Butyl-{(1S,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4-methyl-hept-6-enyloxy}-dimethyl-silane

Guidance literature:: With lithium triethylborohydride; In tetrahydrofuran; at -78 - 20 ℃;
DOI:10.1002/1521-3773(20001201)39:23<4308::AID-ANIE4308>3.0.CO;2-4

Reference yield:

: 128461-65-4
3-(p-methoxybenzyloxy)propanal

: 325172-43-8
tert-Butyl-{(1S,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4-methyl-hept-6-enyloxy}-dimethyl-silane

Guidance literature:: Multi-step reaction with 9 steps

1.1: diethyl ether / -78 °C

1.2: 96 percent / NaOOH / diethyl ether

2.1: 94 percent / imidazole; DMAP / dimethylformamide

3.1: 4-methylmorpholine N-oxide; aq. OsO₄ / acetone

4.1: Pb(OAc)4; pyridine / benzene

5.1: TiCl₄; i-Pr₂NEt / CH₂Cl₂ / -78 °C

5.2: 95 percent / CH₂Cl₂ / -78 °C

6.1: 91 percent / NaI; i-Pr₂NEt / CH₂Cl₂

7.1: 82 percent / LiEt₃BH / tetrahydrofuran / -78 - 20 °C

8.1: 91 percent / Et₃N; DMAP / CH₂Cl₂

9.1: 90 percent / LiEt₃BH / tetrahydrofuran / -78 - 20 °C

With pyridine; 1H-imidazole; lead(IV) acetate; dmap; osmium(VIII) oxide; titanium tetrachloride; lithium triethylborohydride; 4-methylmorpholine N-oxide; triethylamine; N-ethyl-N,N-diisopropylamine; sodium iodide; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1002/1521-3773(20001201)39:23<4308::AID-ANIE4308>3.0.CO;2-4

Reference yield:

: 325172-29-0
(3R)-1-[(4-methoxybenzyl)oxy]hex-5-en-3-ol

: 325172-43-8
tert-Butyl-{(1S,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4-methyl-hept-6-enyloxy}-dimethyl-silane

Guidance literature:: Multi-step reaction with 8 steps

1.1: 94 percent / imidazole; DMAP / dimethylformamide

2.1: 4-methylmorpholine N-oxide; aq. OsO₄ / acetone

3.1: Pb(OAc)4; pyridine / benzene

4.1: TiCl₄; i-Pr₂NEt / CH₂Cl₂ / -78 °C

4.2: 95 percent / CH₂Cl₂ / -78 °C

5.1: 91 percent / NaI; i-Pr₂NEt / CH₂Cl₂

6.1: 82 percent / LiEt₃BH / tetrahydrofuran / -78 - 20 °C

7.1: 91 percent / Et₃N; DMAP / CH₂Cl₂

8.1: 90 percent / LiEt₃BH / tetrahydrofuran / -78 - 20 °C

With pyridine; 1H-imidazole; lead(IV) acetate; dmap; osmium(VIII) oxide; titanium tetrachloride; lithium triethylborohydride; 4-methylmorpholine N-oxide; triethylamine; N-ethyl-N,N-diisopropylamine; sodium iodide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1002/1521-3773(20001201)39:23<4308::AID-ANIE4308>3.0.CO;2-4