(4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one

Base Information

Chemical Name:(4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one
CAS No.:637337-44-1
Molecular Formula:C₂₄H₂₈BrNO₃
Molecular Weight:458.395
Hs Code.:

Synonyms:(4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one

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Chemical Property of (4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one

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Technology Process of (4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one

There total 1 articles about (4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one 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: 88.9%

: 22809-37-6
6-bromohexanoyl chloride

: 191090-32-1
(R)-4-(1-methylethyl)-5,5-diphenyl-1,3-oxazolidin-2-one

: 637337-44-1
(4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one

Guidance literature:: (R)-4-(1-methylethyl)-5,5-diphenyl-1,3-oxazolidin-2-one; With n-butyllithium; In tetrahydrofuran; hexane; at -50 - 30 ℃; Inert atmosphere;

6-bromohexanoyl chloride; In tetrahydrofuran; hexane; at -30 - 20 ℃; Inert atmosphere;
DOI:10.1002/hlca.200900401

Reference yield: 63.9%

: 1220596-99-5
benzyl N-[(benzyloxy)methyl]carbamate

: 637337-44-1
(4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one

: 637337-60-1
(4R)-3-[(2S)-2-({[(benzyloxy)carbonyl]amino}methyl)-6-bromo-1-oxohexyl]-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one

Guidance literature:: (4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one; With titanium tetrachloride; triethylamine; In dichloromethane; at -50 ℃; for 0.5h; Inert atmosphere; Large scale reaction;

benzyl N-[(benzyloxy)methyl]carbamate; With titanium tetrachloride; In dichloromethane; at -40 - 5 ℃; Inert atmosphere; Large scale reaction;
DOI:10.1002/hlca.200900401

Reference yield:

: 637337-44-1
(4R)-3-(6-bromo-1-oxohexyl)-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one

: (4R)-3-[(2S)-2-({[(benzyloxy)carbonyl]amino}methyl)-6-{[(tert-butoxy)carbonyl]amino}-1-oxohexyl]-4-(1-methylethyl)-5,5-diphenyloxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: TiCl₄; Et₃N / CH₂Cl₂ / 0.5 h / -15 °C

1.2: TiCl₄ / CH₂Cl₂ / 3 h / 0 °C

2.1: 95 percent / NaN₃ / dimethylformamide / 14 h / 20 °C

3.1: 92 percent / H₂ / Lindlar catalyst / methanol / 4 h / 20 °C

With sodium azide; hydrogen; titanium tetrachloride; triethylamine; Lindlar's catalyst; In methanol; dichloromethane; N,N-dimethyl-formamide; 1.1: Mannich reaction;
DOI:10.1002/hlca.200590157