(4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one

Base Information

Chemical Name:(4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one
CAS No.:252558-53-5
Molecular Formula:C₃₄H₅₃N₃O₃Si
Molecular Weight:579.899
Hs Code.:

Synonyms:(4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one

Suppliers and Price of (4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one

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 (4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one

There total 10 articles about (4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one 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: 44.0%

: 194653-99-1
(R)-5-azido-2-ethylpentanal

: 252558-52-4
(3S,7R)-7-(tert-Butyl-diphenyl-silanyloxymethyl)-3-methyl-nonan-2-one

: (4R,5S,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one

: 252558-53-5
(4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one

Guidance literature:: (3S,7R)-7-(tert-Butyl-diphenyl-silanyloxymethyl)-3-methyl-nonan-2-one; With menthone-derived boryl bromide; triethylamine; In methanol; diethyl ether; at 0 ℃; for 5h;

(R)-5-azido-2-ethylpentanal; In diethyl ether; at 4 ℃; for 96h;
DOI:10.1002/(SICI)1521-3773(19991018)38:20<3086::AID-ANIE3086>3.0.CO;2-D

Reference yield:

: 89790-39-6
(2R)-2-Ethyl-4-penten-1-ol

: 252558-53-5
(4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: 83 percent / Et₃N; DMAP / tetrahydrofuran / 12 h / 20 °C

2.1: 9-BBN / tetrahydrofuran / 3 h / 20 °C

2.2: 97 percent / H₂O₂; H₂O; NaOH / tetrahydrofuran / 15 h / 5 °C

3.1: 100 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

4.1: 94 percent / NaI / acetone / 24 h / 20 °C

5.1: 87 percent / LDA; LiCl

6.1: 92 percent

7.1: menthone-derived boryl bromide; Et₃N / diethyl ether; methanol / 5 h / 0 °C

7.2: 44 percent / diethyl ether / 96 h / 4 °C

With dmap; 9-borabicyclo[3.3.1]nonane dimer; menthone-derived boryl bromide; triethylamine; sodium iodide; lithium chloride; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetone; 1.1: Etherification / 2.1: Addition / 2.2: Oxidation / 3.1: Esterification / 4.1: Substitution / 5.1: Metallation / 5.2: Alkylation / 6.1: Methylation / 7.1: Substitution / 7.2: Alkylation;
DOI:10.1002/(SICI)1521-3773(19991018)38:20<3086::AID-ANIE3086>3.0.CO;2-D

Reference yield:

: 252558-58-0
tert-butyl-(2-ethyl-pent-4-enyloxy)-diphenyl-silane

: 252558-53-5
(4R,5R,8S,12R)-1-Azido-12-(tert-butyl-diphenyl-silanyloxymethyl)-4-ethyl-5-hydroxy-8-methyl-tetradecan-7-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: 9-BBN / tetrahydrofuran / 3 h / 20 °C

1.2: 97 percent / H₂O₂; H₂O; NaOH / tetrahydrofuran / 15 h / 5 °C

2.1: 100 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

3.1: 94 percent / NaI / acetone / 24 h / 20 °C

4.1: 87 percent / LDA; LiCl

5.1: 92 percent

6.1: menthone-derived boryl bromide; Et₃N / diethyl ether; methanol / 5 h / 0 °C

6.2: 44 percent / diethyl ether / 96 h / 4 °C

With 9-borabicyclo[3.3.1]nonane dimer; menthone-derived boryl bromide; triethylamine; sodium iodide; lithium chloride; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetone; 1.1: Addition / 1.2: Oxidation / 2.1: Esterification / 3.1: Substitution / 4.1: Metallation / 4.2: Alkylation / 5.1: Methylation / 6.1: Substitution / 6.2: Alkylation;
DOI:10.1002/(SICI)1521-3773(19991018)38:20<3086::AID-ANIE3086>3.0.CO;2-D