2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime

Base Information

Chemical Name:2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime
CAS No.:488759-23-5
Molecular Formula:C₂₀H₂₁NO₃S
Molecular Weight:355.458
Hs Code.:

2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde <i>O</i>-benzyl-oxime

Synonyms:2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime

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Chemical Property of 2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime

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Technology Process of 2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime

There total 4 articles about 2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime 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: 50.0%

: 488759-27-9
2-(4-methylsulfanyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime

: 488759-23-5
2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime

Guidance literature:: With potassium hydrogensulfate; potassium peroxomonosulfate; potassium carbonate; In tetrahydrofuran; methanol; water; at 20 ℃; for 12h;
DOI:10.1016/S0223-5234(02)01359-4

Reference yield:

: 89466-25-1
1-bromo-2-formylcyclopentene

: 488759-23-5
2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / CHCl₃; H₂O / 24 h / 20 °C

2: 51 percent / Na₂CO₃; Pd(PPh₃)4 / H₂O; toluene; ethanol / 12 h / Heating

3: 50 percent / 2KHSO₅*KHSO₄*K₂CO₃ / H₂O; methanol; tetrahydrofuran / 12 h / 20 °C

With potassium hydrogensulfate; potassium peroxomonosulfate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; potassium carbonate; In tetrahydrofuran; methanol; ethanol; chloroform; water; toluene;
DOI:10.1016/S0223-5234(02)01359-4

Reference yield:

: 2687-43-6
O-benzylhydoxylamine hydrochloride

: 488759-23-5
2-(4-methanesulfonyl-phenyl)-cyclopent-1-enecarbaldehyde O-benzyl-oxime

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / CHCl₃; H₂O / 24 h / 20 °C

2: 51 percent / Na₂CO₃; Pd(PPh₃)4 / H₂O; toluene; ethanol / 12 h / Heating

3: 50 percent / 2KHSO₅*KHSO₄*K₂CO₃ / H₂O; methanol; tetrahydrofuran / 12 h / 20 °C

With potassium hydrogensulfate; potassium peroxomonosulfate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; potassium carbonate; In tetrahydrofuran; methanol; ethanol; chloroform; water; toluene;
DOI:10.1016/S0223-5234(02)01359-4