Acetic acid (1S,4R)-4-(1-benzenesulfonyl-2-oxo-2-phenyl-ethyl)-1-butyl-cyclopent-2-enyl ester

Base Information

Chemical Name:Acetic acid (1S,4R)-4-(1-benzenesulfonyl-2-oxo-2-phenyl-ethyl)-1-butyl-cyclopent-2-enyl ester
CAS No.:934976-57-5
Molecular Formula:C₂₅H₂₈O₅S
Molecular Weight:440.56
Hs Code.:

Synonyms:Acetic acid (1S,4R)-4-(1-benzenesulfonyl-2-oxo-2-phenyl-ethyl)-1-butyl-cyclopent-2-enyl ester

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Chemical Property of Acetic acid (1S,4R)-4-(1-benzenesulfonyl-2-oxo-2-phenyl-ethyl)-1-butyl-cyclopent-2-enyl ester

Chemical Property:

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Technology Process of Acetic acid (1S,4R)-4-(1-benzenesulfonyl-2-oxo-2-phenyl-ethyl)-1-butyl-cyclopent-2-enyl ester

There total 5 articles about Acetic acid (1S,4R)-4-(1-benzenesulfonyl-2-oxo-2-phenyl-ethyl)-1-butyl-cyclopent-2-enyl 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:

: 59995-48-1
(R)-4-acetoxycyclopent-2-en-1-one

: 934976-57-5
Acetic acid (1S,4R)-4-(1-benzenesulfonyl-2-oxo-2-phenyl-ethyl)-1-butyl-cyclopent-2-enyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: diethyl ether / 1 h / -78 °C

2: DMAP / tetrahydrofuran / 3 h / 20 °C

3: 73 percent / potassium carbonate; triphenylphosphine / Pd(PPh₃)4 / tetrahydrofuran / 12 h / 40 °C

4: DMAP / tetrahydrofuran / 3 h / 20 °C

With dmap; potassium carbonate; triphenylphosphine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; diethyl ether;
DOI:10.1016/j.tet.2006.11.066

Reference yield:

: 926920-26-5
(1S,4R)-1-butyl-cyclopent-2-ene-1,4-diol

: 934976-57-5
Acetic acid (1S,4R)-4-(1-benzenesulfonyl-2-oxo-2-phenyl-ethyl)-1-butyl-cyclopent-2-enyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: DMAP / tetrahydrofuran / 3 h / 20 °C

2: 73 percent / potassium carbonate; triphenylphosphine / Pd(PPh₃)4 / tetrahydrofuran / 12 h / 40 °C

3: DMAP / tetrahydrofuran / 3 h / 20 °C

With dmap; potassium carbonate; triphenylphosphine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran;
DOI:10.1016/j.tet.2006.11.066

Reference yield:

: 926920-38-9
(1R,4S)-4-hydroxy-4-butyl-2-cyclopenten-1-yl acetate

: 934976-57-5
Acetic acid (1S,4R)-4-(1-benzenesulfonyl-2-oxo-2-phenyl-ethyl)-1-butyl-cyclopent-2-enyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / potassium carbonate; triphenylphosphine / Pd(PPh₃)4 / tetrahydrofuran / 12 h / 40 °C

2: DMAP / tetrahydrofuran / 3 h / 20 °C

With dmap; potassium carbonate; triphenylphosphine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran;
DOI:10.1016/j.tet.2006.11.066