(4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester

Base Information

Chemical Name:(4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester
CAS No.:748793-59-1
Molecular Formula:C₁₉H₂₉NO₄
Molecular Weight:335.444
Hs Code.:

Synonyms:(4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester

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Chemical Property of (4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester

Chemical Property:

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Safty Information:

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MSDS Files:: SDS file from LookChem

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Technology Process of (4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester

There total 4 articles about (4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl 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:

: 4248-19-5
tert-butyl carbazate

: 99773-69-0
(E)-2-hydroxy-2-methyl-7-phenyl-hept-4-en-3-one

: 748793-59-1
(4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester

: (4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester

Guidance literature:: (E)-2-hydroxy-2-methyl-7-phenyl-hept-4-en-3-one; With 2,2'-isopropylidenebis<(4S)-4-tert-butyl-4,5-dihydrooxazole>; copper(II) bis(trifluoromethanesulfonate); In dichloromethane; at 20 ℃; for 0.5h;

tert-butyl carbazate; In dichloromethane; at 20 ℃; for 18h; Title compound not separated from byproducts;
DOI:10.1021/ja047004e

Reference yield:

: 104-53-0
3-phenyl-propionaldehyde

: 748793-59-1
(4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: LDA / tetrahydrofuran; hexane / 1 h / -78 °C

1.2: tetrahydrofuran; hexane / -78 °C

2.1: 7.7 g / CeCl₃*7H₂O; NaI / acetonitrile / 3 h / Heating

3.1: 2,2'-isopropylidene bis[(4S)-4-tert-butyl-2-oxazoline]; Cu(OTf)2 / CH₂Cl₂ / 0.5 h / 20 °C

3.2: CH₂Cl₂ / 18 h / 20 °C

With cerium(III) chloride; 2,2'-isopropylidenebis<(4S)-4-tert-butyl-4,5-dihydrooxazole>; copper(II) bis(trifluoromethanesulfonate); sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; hexane; dichloromethane; acetonitrile;
DOI:10.1021/ja047004e

Reference yield:

: 115-22-0
3-Hydroxy-3-methyl-2-butanone

: 748793-59-1
(4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: LDA / tetrahydrofuran; hexane / 1 h / -78 °C

1.2: tetrahydrofuran; hexane / -78 °C

2.1: 7.7 g / CeCl₃*7H₂O; NaI / acetonitrile / 3 h / Heating

3.1: 2,2'-isopropylidene bis[(4S)-4-tert-butyl-2-oxazoline]; Cu(OTf)2 / CH₂Cl₂ / 0.5 h / 20 °C

3.2: CH₂Cl₂ / 18 h / 20 °C

With cerium(III) chloride; 2,2'-isopropylidenebis<(4S)-4-tert-butyl-4,5-dihydrooxazole>; copper(II) bis(trifluoromethanesulfonate); sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; hexane; dichloromethane; acetonitrile;
DOI:10.1021/ja047004e