(R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-one

Base Information

Chemical Name:(R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-one
CAS No.:955406-64-1
Molecular Formula:C₂₈H₂₄Cl₂FNO₃
Molecular Weight:512.408
Hs Code.:

Synonyms:(R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-one

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Chemical Property of (R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-one

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Technology Process of (R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-one

There total 7 articles about (R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-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:

: 955406-57-2
4-bromomethyl-3,5-dichloro-4'-fluoro-biphenyl

: 155399-10-3
(4R)-3-(4-pentenoyl)-4-(phenylmethyl)-1,3-oxazolidin-2-one

: 955406-64-1
(R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-one

Guidance literature:: (4R)-3-(4-pentenoyl)-4-(phenylmethyl)-1,3-oxazolidin-2-one; With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 - -25 ℃; for 1.16667h; Cooling with acetone-dry ice;

4-bromomethyl-3,5-dichloro-4'-fluoro-biphenyl; In tetrahydrofuran; at -78 - 20 ℃; Cooling with acetone-dry ice;

Reference yield:

: 118-69-4
2,6-dichlorotoluene

: 955406-64-1
(R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: [2,2]bipyridinyl / chloro(1,5-cyclooctadiene)iridium(I) dimer / n-heptane / 4 h / 100 °C

2.1: potassium carbonate / palladium diacetate; triphenylphosphine / water; isopropyl alcohol / 8 h / 75 °C

3.1: N-Bromosuccinimide; dibenzoyl peroxide / chlorobenzene / 1 - 2 h / 85 - 120 °C

4.1: lithium hexamethyldisilazane / tetrahydrofuran / 1.17 h / -78 - -25 °C / Cooling with acetone-dry ice

4.2: -78 - 20 °C / Cooling with acetone-dry ice

With [2,2]bipyridinyl; N-Bromosuccinimide; potassium carbonate; lithium hexamethyldisilazane; dibenzoyl peroxide; palladium diacetate; chloro(1,5-cyclooctadiene)iridium(I) dimer; triphenylphosphine; In tetrahydrofuran; n-heptane; water; chlorobenzene; isopropyl alcohol;

Reference yield:

: 942069-73-0
2-(3,5-dichloro-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

: 955406-64-1
(R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / palladium diacetate; triphenylphosphine / water; isopropyl alcohol / 8 h / 75 °C

2.1: N-Bromosuccinimide; dibenzoyl peroxide / chlorobenzene / 1 - 2 h / 85 - 120 °C

3.1: lithium hexamethyldisilazane / tetrahydrofuran / 1.17 h / -78 - -25 °C / Cooling with acetone-dry ice

3.2: -78 - 20 °C / Cooling with acetone-dry ice

With N-Bromosuccinimide; potassium carbonate; lithium hexamethyldisilazane; dibenzoyl peroxide; palladium diacetate; triphenylphosphine; In tetrahydrofuran; water; chlorobenzene; isopropyl alcohol;