(3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-1,4-diol

Base Information

Chemical Name:(3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-1,4-diol
CAS No.:457613-98-8
Molecular Formula:C₂₃H₃₇NO₇
Molecular Weight:439.549
Hs Code.:

Synonyms:(3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-1,4-diol

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Chemical Property of (3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-1,4-diol

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Technology Process of (3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-1,4-diol

There total 4 articles about (3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-1,4-diol 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:

: 457613-96-6
(3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)-4-[(triethylsilyl)oxy]hex-1-ene

: (3S,3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-2,4-diol

: 457613-98-8
(3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-1,4-diol

Guidance literature:: (3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)-4-[(triethylsilyl)oxy]hex-1-ene; With borane; In tetrahydrofuran; at 0 - 20 ℃; for 4h;

With sodium hydroxide; dihydrogen peroxide; at 20 ℃; for 2h;

With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃;
DOI:10.1055/s-2002-28505

Reference yield:

: 13391-35-0
allyl (4-methoxyphenyl) ether

: 457613-98-8
(3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-1,4-diol

Guidance literature:: Multi-step reaction with 3 steps

1.1: sec-BuLi / tetrahydrofuran; cyclohexane / 0.42 h / -78 °C

1.2: chiral cyclopentadienyl titanium complex / tetrahydrofuran; cyclohexane; diethyl ether / 3 h / -78 °C

1.3: 69 percent / tetrahydrofuran; cyclohexane; diethyl ether / 4 h / -78 °C

2.1: 87 percent / imidazole / CH₂Cl₂ / 20 °C

3.1: BH₃ / tetrahydrofuran / 4 h / 0 - 20 °C

3.2: aq. H₂O₂; NaOH / 2 h / 20 °C

3.3: 1.56 g / TBAF / tetrahydrofuran / 20 °C

With 1H-imidazole; borane; sec.-butyllithium; In tetrahydrofuran; dichloromethane; cyclohexane;
DOI:10.1055/s-2002-28505

Reference yield:

: 144090-56-2
2,2-dimethyl-3-<(1,1-dimethylethoxy)carbonyl>-4(S)-oxazolidinepropanal

: 457613-98-8
(3S,4R)-6-[(4S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidin-4-yl]-3-(4-methoxyphenoxy)hexan-1,4-diol

Guidance literature:: Multi-step reaction with 3 steps

1.1: sec-BuLi / tetrahydrofuran; cyclohexane / 0.42 h / -78 °C

1.2: chiral cyclopentadienyl titanium complex / tetrahydrofuran; cyclohexane; diethyl ether / 3 h / -78 °C

1.3: 69 percent / tetrahydrofuran; cyclohexane; diethyl ether / 4 h / -78 °C

2.1: 87 percent / imidazole / CH₂Cl₂ / 20 °C

3.1: BH₃ / tetrahydrofuran / 4 h / 0 - 20 °C

3.2: aq. H₂O₂; NaOH / 2 h / 20 °C

3.3: 1.56 g / TBAF / tetrahydrofuran / 20 °C

With 1H-imidazole; borane; sec.-butyllithium; In tetrahydrofuran; dichloromethane; cyclohexane;
DOI:10.1055/s-2002-28505