1-[2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]phenyl]-6,6-dimethyl-6-silahepta-2,4-diyn-1-ol

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Chemical Name:1-[2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]phenyl]-6,6-dimethyl-6-silahepta-2,4-diyn-1-ol
CAS No.:341970-27-2
Molecular Formula:C₄₃H₄₁NO₃Si
Molecular Weight:647.889
Hs Code.:

Synonyms:1-[2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]phenyl]-6,6-dimethyl-6-silahepta-2,4-diyn-1-ol

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Chemical Property of 1-[2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]phenyl]-6,6-dimethyl-6-silahepta-2,4-diyn-1-ol

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Technology Process of 1-[2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]phenyl]-6,6-dimethyl-6-silahepta-2,4-diyn-1-ol

There total 5 articles about 1-[2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]phenyl]-6,6-dimethyl-6-silahepta-2,4-diyn-1-ol 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: 98.0%

: 4526-07-2
1,4-bis(trimethylsilyl)-1,3-butadiyne

: 341970-24-9
2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]benzaldehyde

: 341970-27-2
1-[2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]phenyl]-6,6-dimethyl-6-silahepta-2,4-diyn-1-ol

Guidance literature:: With methyllithium; lithium bromide; In diethyl ether; at 20 ℃; for 0.0833333h;
DOI:10.3987/com-00-s(i)88

Reference yield:

: 21420-61-1
N-(tert-butoxycarbonyl)(diphenylmethyl)amine

: 341970-27-2
1-[2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]phenyl]-6,6-dimethyl-6-silahepta-2,4-diyn-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / NaH / dimethylformamide / 4 h / 0 - 20 °C

2: 79 percent / Pd₂Cl₂(PPh₃)2 / toluene / 2 h / 110 °C

3: 92 percent / 2-iodoxybenzoic acid / dimethylsulfoxide / 0.5 h / 20 °C

4: 98 percent / MeLi-LiBr / diethyl ether / 0.08 h / 20 °C

With methyllithium; sodium hydride; lithium bromide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; Pd₂(PPh₃)2Cl₂; In diethyl ether; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
DOI:10.3987/com-00-s(i)88

Reference yield:

: 4622-38-2
2-iodobenzyliodide

: 341970-27-2
1-[2-[4-(2-N-tert-butoxycarbonyl-N-diphenylmethylaminomethylphenyl)buta-1,3-diyn-1-yl]phenyl]-6,6-dimethyl-6-silahepta-2,4-diyn-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / NaH / dimethylformamide / 4 h / 0 - 20 °C

2: 79 percent / Pd₂Cl₂(PPh₃)2 / toluene / 2 h / 110 °C

3: 92 percent / 2-iodoxybenzoic acid / dimethylsulfoxide / 0.5 h / 20 °C

4: 98 percent / MeLi-LiBr / diethyl ether / 0.08 h / 20 °C

With methyllithium; sodium hydride; lithium bromide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; Pd₂(PPh₃)2Cl₂; In diethyl ether; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
DOI:10.3987/com-00-s(i)88