1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine

Base Information

Chemical Name:1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine
CAS No.:203438-50-0
Molecular Formula:C₂₄H₂₉ClINO₄
Molecular Weight:557.856
Hs Code.:

Synonyms:1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine

Suppliers and Price of 1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine

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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-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine

Chemical Property:

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Technology Process of 1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine

There total 6 articles about 1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine 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: 63.0%

: 203438-49-7
1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-3-methoxyphenyl)piperidine

: 203438-50-0
1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine

Guidance literature:: With Iodine monochloride; triethylamine; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1002/hlca.19980810112

Reference yield:

: 32161-06-1
1-acetyl-4-piperidinone

: 203438-50-0
1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine

Guidance literature:: Multi-step reaction with 5 steps

1: 56 percent / Mg / tetrahydrofuran / 2 h / Ambient temperature

2: 98 percent / BBr₃ / CH₂Cl₂ / 3 h / Heating

3: 74 percent / K₂CO₃ / acetonitrile / 28 h / Heating

4: 68 percent / BF₃*Et₂O / CH₂Cl₂ / 216 h / Ambient temperature

5: 63 percent / ICl, NEt₃ / CH₂Cl₂ / 2 h / 0 °C

With boron trifluoride diethyl etherate; Iodine monochloride; boron tribromide; potassium carbonate; magnesium; triethylamine; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1002/hlca.19980810112

Reference yield:

: 104-92-7
1-bromo-4-methoxy-benzene

: 203438-50-0
1-acetyl-4-[4-(4-chlorobutoxy)phenyl]-4-(4-hydroxy-5-iodo-3-methoxyphenyl)piperidine

Guidance literature:: Multi-step reaction with 5 steps

1: 56 percent / Mg / tetrahydrofuran / 2 h / Ambient temperature

2: 98 percent / BBr₃ / CH₂Cl₂ / 3 h / Heating

3: 74 percent / K₂CO₃ / acetonitrile / 28 h / Heating

4: 68 percent / BF₃*Et₂O / CH₂Cl₂ / 216 h / Ambient temperature

5: 63 percent / ICl, NEt₃ / CH₂Cl₂ / 2 h / 0 °C

With boron trifluoride diethyl etherate; Iodine monochloride; boron tribromide; potassium carbonate; magnesium; triethylamine; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1002/hlca.19980810112