1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene

Base Information

Chemical Name:1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene
CAS No.:141462-37-5
Molecular Formula:C₂₄H₃₀O₃
Molecular Weight:366.5
Hs Code.:

Synonyms:1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene

Suppliers and Price of 1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene

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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 1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene

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Technology Process of 1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene

There total 3 articles about 1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene 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: 46.0%

: 109-72-8,29786-93-4
n-butyllithium

: 141462-35-3
3-Isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutenone

: 141462-37-5
1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene

Guidance literature:: In hexane; at -78 ℃; for 1h;
DOI:10.1021/jo00042a009

Reference yield:

: 591-51-5
phenyllithium

: 141462-37-5
1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene

Guidance literature:: Multi-step reaction with 3 steps

1: 56 percent / tetrahydrofuran / 1 h / -78 °C

2: 95 percent / Ag₂O, K₂CO₃ / acetonitrile / Ambient temperature

3: 46 percent / hexane / 1 h / -78 °C

With potassium carbonate; silver(l) oxide; In tetrahydrofuran; hexane; acetonitrile;
DOI:10.1021/jo00042a009

Reference yield:

: 141462-26-2
3-Isopropoxy-2-phenyl-4-hydroxy-4-phenyl-2-cyclobutenone

: 141462-37-5
1-n-Butyl-1-hydroxy-3-isopropoxy-2-phenyl-4-methoxy-4-phenyl-2-cyclobutene

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / Ag₂O, K₂CO₃ / acetonitrile / Ambient temperature

2: 46 percent / hexane / 1 h / -78 °C

With potassium carbonate; silver(l) oxide; In hexane; acetonitrile;
DOI:10.1021/jo00042a009