C₂₇H₄₈O₆Si

Base Information

Chemical Name:C₂₇H₄₈O₆Si
CAS No.:1426324-35-7
Molecular Formula:C₂₇H₄₈O₆Si
Molecular Weight:496.76
Hs Code.:

C<sub>27</sub>H<sub>48</sub>O<sub>6</sub>Si

Synonyms:C₂₇H₄₈O₆Si

Suppliers and Price of C₂₇H₄₈O₆Si

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₂₇H₄₈O₆Si

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₇H₄₈O₆Si

There total 10 articles about C₂₇H₄₈O₆Si 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:

: 1426324-32-4
C₂₄H₄₂O₅Si

: 123-38-6
propionaldehyde

: 1426324-35-7
C₂₇H₄₈O₆Si

Guidance literature:: propionaldehyde; With samarium diiodide; In tetrahydrofuran; at -30 ℃; for 0.166667h;

C₂₄H₄₂O₅Si; In tetrahydrofuran; at -30 ℃; for 2h; diastereoselective reaction;
DOI:10.1021/ol400280b

Reference yield:

: 136320-64-4
(2R)-3-[(4-methoxybenzyl)oxy]-2-methylpropanol

: 1426324-35-7
C₂₇H₄₈O₆Si

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / dichloromethane / 2 h / 0 - 20 °C

2.1: sodium iodide / acetone / 4 h / 60 °C

3.1: tetrahydrofuran; pentane; N,N,N,N,N,N-hexamethylphosphoric triamide / 1.5 h / -78 °C

3.2: 3.5 h / -78 °C

4.1: iodine; sodium hydrogencarbonate / tetrahydrofuran; water / 1.17 h / 0 - 20 °C

5.1: (+)-diisopinocampheylborane trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane; hexane / 3.5 h / -78 - -30 °C

5.2: 13 h / -78 - -20 °C

5.3: 2.5 h / 0 - 20 °C

6.1: samarium diiodide / tetrahydrofuran / 0.17 h / -30 °C

6.2: 2 h / -30 °C

With samarium diiodide; iodine; sodium hydrogencarbonate; (+)-diisopinocampheylborane trifluoromethanesulfonate; triethylamine; N-ethyl-N,N-diisopropylamine; sodium iodide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; dichloromethane; water; acetone; pentane; 6.1: |Evans Aldol Reaction / 6.2: |Evans Aldol Reaction;
DOI:10.1021/ol400280b

Reference yield:

: 136320-73-5
Methanesulfonic acid (S)-3-(4-methoxy-benzyloxy)-2-methyl-propyl ester

: 1426324-35-7
C₂₇H₄₈O₆Si

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium iodide / acetone / 4 h / 60 °C

2.1: tetrahydrofuran; pentane; N,N,N,N,N,N-hexamethylphosphoric triamide / 1.5 h / -78 °C

2.2: 3.5 h / -78 °C

3.1: iodine; sodium hydrogencarbonate / tetrahydrofuran; water / 1.17 h / 0 - 20 °C

4.1: (+)-diisopinocampheylborane trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane; hexane / 3.5 h / -78 - -30 °C

4.2: 13 h / -78 - -20 °C

4.3: 2.5 h / 0 - 20 °C

5.1: samarium diiodide / tetrahydrofuran / 0.17 h / -30 °C

5.2: 2 h / -30 °C

With samarium diiodide; iodine; sodium hydrogencarbonate; (+)-diisopinocampheylborane trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine; sodium iodide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; dichloromethane; water; acetone; pentane; 5.1: |Evans Aldol Reaction / 5.2: |Evans Aldol Reaction;
DOI:10.1021/ol400280b