3-benzyloxy-1-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl)-2-methyl-4(1H)-pyridinone

Base Information

Chemical Name:3-benzyloxy-1-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl)-2-methyl-4(1H)-pyridinone
CAS No.:224564-29-8
Molecular Formula:C₃₀H₃₉NO₃
Molecular Weight:461.645
Hs Code.:

Synonyms:3-benzyloxy-1-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl)-2-methyl-4(1H)-pyridinone

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Chemical Property of 3-benzyloxy-1-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl)-2-methyl-4(1H)-pyridinone

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Technology Process of 3-benzyloxy-1-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl)-2-methyl-4(1H)-pyridinone

There total 5 articles about 3-benzyloxy-1-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl)-2-methyl-4(1H)-pyridinone 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: 40.0%

: 61049-69-2
3-O-benzylmaltol

: 19510-14-6
γ-(4-hydroxy-3,5-di-tert-butylphenyl)propylamine

: 224564-29-8
3-benzyloxy-1-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl)-2-methyl-4(1H)-pyridinone

Guidance literature:: With sodium hydroxide; In ethanol; water; for 4.5h; Heating;
DOI:10.1021/jm990945v

Reference yield:

: 95602-92-9
3,5-di-tert-butyl-4-hydroxycinnamic acid

: 224564-29-8
3-benzyloxy-1-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl)-2-methyl-4(1H)-pyridinone

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / H₂ / Pd/C / ethanol / 3 h / 20 °C / 2585.81 Torr

2: thionyl chloride; DMF / toluene; CH₂Cl₂ / 2 h / 20 °C

3: 28.6 g / NH₄OH / tetrahydrofuran / 0.25 h / 0 °C

4: 45 percent / LiAlH₄ / diethyl ether / 5.5 h / Heating

5: 40 percent / NaOH / ethanol; H₂O / 4.5 h / Heating

With ammonium hydroxide; sodium hydroxide; lithium aluminium tetrahydride; thionyl chloride; hydrogen; N,N-dimethyl-formamide; palladium on activated charcoal; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; water; toluene; 1: Catalytic hydrogenation / 2: Chlorination / 3: Acylation / 4: Reduction / 5: Condensation;
DOI:10.1021/jm990945v

Reference yield:

: 20170-32-5,90804-34-5
4-hydroxy-3,5-di-tert-butylphenylpropionic acid

: 224564-29-8
3-benzyloxy-1-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl)-2-methyl-4(1H)-pyridinone

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride; DMF / toluene; CH₂Cl₂ / 2 h / 20 °C

2: 28.6 g / NH₄OH / tetrahydrofuran / 0.25 h / 0 °C

3: 45 percent / LiAlH₄ / diethyl ether / 5.5 h / Heating

4: 40 percent / NaOH / ethanol; H₂O / 4.5 h / Heating

With ammonium hydroxide; sodium hydroxide; lithium aluminium tetrahydride; thionyl chloride; N,N-dimethyl-formamide; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; water; toluene; 1: Chlorination / 2: Acylation / 3: Reduction / 4: Condensation;
DOI:10.1021/jm990945v