(1S,2S)-1,2-Bis(benzoyloxy)-4-diphenylphosphinoyl-1-(4-methoxyphenyl)butane

Base Information

Chemical Name:(1S,2S)-1,2-Bis(benzoyloxy)-4-diphenylphosphinoyl-1-(4-methoxyphenyl)butane
CAS No.:335274-33-4
Molecular Formula:C₃₇H₃₃O₆P
Molecular Weight:604.639
Hs Code.:

Synonyms:(1S,2S)-1,2-Bis(benzoyloxy)-4-diphenylphosphinoyl-1-(4-methoxyphenyl)butane

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (1S,2S)-1,2-Bis(benzoyloxy)-4-diphenylphosphinoyl-1-(4-methoxyphenyl)butane

Chemical Property:

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Technology Process of (1S,2S)-1,2-Bis(benzoyloxy)-4-diphenylphosphinoyl-1-(4-methoxyphenyl)butane

There total 4 articles about (1S,2S)-1,2-Bis(benzoyloxy)-4-diphenylphosphinoyl-1-(4-methoxyphenyl)butane 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: 57.0%

: 98-88-4
benzoyl chloride

: 335274-26-5
(1S,2S)-4-Diphenylphosphinoyl-1-(4-methoxyphenyl)butane-1,2-diol

: 335274-33-4
(1S,2S)-1,2-Bis(benzoyloxy)-4-diphenylphosphinoyl-1-(4-methoxyphenyl)butane

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 8h;
DOI:10.1039/b008500f

Reference yield:

: 53484-50-7
(E)-p-methoxy-cinnamyl alcohol

: 335274-33-4
(1S,2S)-1,2-Bis(benzoyloxy)-4-diphenylphosphinoyl-1-(4-methoxyphenyl)butane

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaI; Me₃SiCl / tetrahydrofuran / 1 h / 20 °C

2.1: nBuLi / tetrahydrofuran; hexane / 1 h / 0 °C

2.2: tetrahydrofuran; hexane / 9 h / -78 °C

3.1: 58 percent / AD-mix-α; methanesulfonamide / H2O; 2-methyl-propan-2-ol / 120 h

4.1: 57 percent / Et₃N; DMAP / CH₂Cl₂ / 8 h / 20 °C

With dmap; AD-mix-α; n-butyllithium; chloro-trimethyl-silane; methanesulfonamide; triethylamine; sodium iodide; In tetrahydrofuran; hexane; dichloromethane; water; tert-butyl alcohol;
DOI:10.1039/b008500f

Reference yield:

: 1-((E)-3-Iodo-propenyl)-4-methoxy-benzene

: 335274-33-4
(1S,2S)-1,2-Bis(benzoyloxy)-4-diphenylphosphinoyl-1-(4-methoxyphenyl)butane

Guidance literature:: Multi-step reaction with 3 steps

1.1: nBuLi / tetrahydrofuran; hexane / 1 h / 0 °C

1.2: tetrahydrofuran; hexane / 9 h / -78 °C

2.1: 58 percent / AD-mix-α; methanesulfonamide / H2O; 2-methyl-propan-2-ol / 120 h

3.1: 57 percent / Et₃N; DMAP / CH₂Cl₂ / 8 h / 20 °C

With dmap; AD-mix-α; n-butyllithium; methanesulfonamide; triethylamine; In tetrahydrofuran; hexane; dichloromethane; water; tert-butyl alcohol;
DOI:10.1039/b008500f