1-(4-benzyloxyphenoxy)-8-[2-(N-tert-butoxycarbonylamino)-2-phenyl-1-ethyloxy]octane

Base Information

Chemical Name:1-(4-benzyloxyphenoxy)-8-[2-(N-tert-butoxycarbonylamino)-2-phenyl-1-ethyloxy]octane
CAS No.:943151-77-7
Molecular Formula:C₃₄H₄₅NO₅
Molecular Weight:547.735
Hs Code.:

Synonyms:1-(4-benzyloxyphenoxy)-8-[2-(N-tert-butoxycarbonylamino)-2-phenyl-1-ethyloxy]octane

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Chemical Property of 1-(4-benzyloxyphenoxy)-8-[2-(N-tert-butoxycarbonylamino)-2-phenyl-1-ethyloxy]octane

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Technology Process of 1-(4-benzyloxyphenoxy)-8-[2-(N-tert-butoxycarbonylamino)-2-phenyl-1-ethyloxy]octane

There total 4 articles about 1-(4-benzyloxyphenoxy)-8-[2-(N-tert-butoxycarbonylamino)-2-phenyl-1-ethyloxy]octane 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:

: C₂₂F₃H₂₇O₅S

: 117049-14-6
tert-butyl N-[(1S)-2-hydroxy-1-phenylethyl]carbamate

: 943151-77-7
1-(4-benzyloxyphenoxy)-8-[2-(N-tert-butoxycarbonylamino)-2-phenyl-1-ethyloxy]octane

Guidance literature:: C₂₂F₃H₂₇O₅S; tert-butyl N-[(1S)-2-hydroxy-1-phenylethyl]carbamate; With sodium hydride; In dichloromethane; at 0 ℃;

With 18-crown-6 ether; In dichloromethane; at 20 ℃; Further stages.;
DOI:10.1021/jm061349l

Reference yield:

: 50816-19-8
8-bromooctanol

: 943151-77-7
1-(4-benzyloxyphenoxy)-8-[2-(N-tert-butoxycarbonylamino)-2-phenyl-1-ethyloxy]octane

Guidance literature:: Multi-step reaction with 3 steps

1.1: NaH / dimethylformamide / 0.5 h / 20 °C

1.2: 80 percent / dimethylformamide / 3 h / 20 °C

2.1: 2,6-lutidine / CH₂Cl₂ / 0.25 h / 0 °C

3.1: NaH / CH₂Cl₂ / 0 °C

3.2: 0.411 g / 18-crown-6 / CH₂Cl₂ / 20 °C

With 2,6-dimethylpyridine; sodium hydride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm061349l

Reference yield:

: 103-16-2
4-Benzyloxyphenol

: 943151-77-7
1-(4-benzyloxyphenoxy)-8-[2-(N-tert-butoxycarbonylamino)-2-phenyl-1-ethyloxy]octane

Guidance literature:: Multi-step reaction with 3 steps

1.1: NaH / dimethylformamide / 0.5 h / 20 °C

1.2: 80 percent / dimethylformamide / 3 h / 20 °C

2.1: 2,6-lutidine / CH₂Cl₂ / 0.25 h / 0 °C

3.1: NaH / CH₂Cl₂ / 0 °C

3.2: 0.411 g / 18-crown-6 / CH₂Cl₂ / 20 °C

With 2,6-dimethylpyridine; sodium hydride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm061349l