Diisopropyl-carbamic acid (2Z,7Z)-(S)-5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-dienyl ester

Base Information

Chemical Name:Diisopropyl-carbamic acid (2Z,7Z)-(S)-5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-dienyl ester
CAS No.:292170-88-8
Molecular Formula:C₃₂H₄₇NO₄Si
Molecular Weight:537.815
Hs Code.:

Synonyms:Diisopropyl-carbamic acid (2Z,7Z)-(S)-5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-dienyl ester

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Chemical Property of Diisopropyl-carbamic acid (2Z,7Z)-(S)-5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-dienyl ester

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Technology Process of Diisopropyl-carbamic acid (2Z,7Z)-(S)-5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-dienyl ester

There total 4 articles about Diisopropyl-carbamic acid (2Z,7Z)-(S)-5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-dienyl 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: 96.0%

: 292170-87-7
diisopropyl-carbamic acid 5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-diynyl ester

: 292170-88-8
Diisopropyl-carbamic acid (2Z,7Z)-(S)-5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-dienyl ester

Guidance literature:: With quinoline; hydrogen; Lindlar's catalyst; In methanol;
DOI:10.1002/1521-3773(20000616)39:12<2105::AID-ANIE2105>3.0.CO;2-X

Reference yield:

: 292170-84-4
(S)-2-[4-(2-Ethoxy-ethoxy)-but-2-ynyl]-oxirane

: 292170-88-8
Diisopropyl-carbamic acid (2Z,7Z)-(S)-5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-dienyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / nBuLi; BF₃*OEt₂ / tetrahydrofuran / -78 - 20 °C

2: 83 percent / imidazole / toluene

3: 95 percent / amberlyst 15; MeOH / 40 °C

4: 96 percent / H₂; quinoline / 5 percent Lindlar catalyst / methanol

With 1H-imidazole; quinoline; methanol; n-butyllithium; Amberlyst 15; boron trifluoride diethyl etherate; hydrogen; Lindlar's catalyst; In tetrahydrofuran; methanol; toluene; 1: Ring cleavage / 2: Etherification / 3: Ether cleavage / 4: Catalytic hydrogenation;
DOI:10.1002/1521-3773(20000616)39:12<2105::AID-ANIE2105>3.0.CO;2-X

Reference yield:

: 292170-85-5
Diisopropyl-carbamic acid (S)-9-(2-ethoxy-ethoxy)-5-hydroxy-nona-2,7-diynyl ester

: 292170-88-8
Diisopropyl-carbamic acid (2Z,7Z)-(S)-5-(tert-butyl-diphenyl-silanyloxy)-9-hydroxy-nona-2,7-dienyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / imidazole / toluene

2: 95 percent / amberlyst 15; MeOH / 40 °C

3: 96 percent / H₂; quinoline / 5 percent Lindlar catalyst / methanol

With 1H-imidazole; quinoline; methanol; Amberlyst 15; hydrogen; Lindlar's catalyst; In methanol; toluene; 1: Etherification / 2: Ether cleavage / 3: Catalytic hydrogenation;
DOI:10.1002/1521-3773(20000616)39:12<2105::AID-ANIE2105>3.0.CO;2-X