{5-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pentyl}-isobutyl-amine

Base Information

Chemical Name:{5-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pentyl}-isobutyl-amine
CAS No.:869101-66-6
Molecular Formula:C₃₉H₄₉NO₄
Molecular Weight:595.822
Hs Code.:

Synonyms:{5-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pentyl}-isobutyl-amine

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Chemical Property of {5-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pentyl}-isobutyl-amine

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Technology Process of {5-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pentyl}-isobutyl-amine

There total 7 articles about {5-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pentyl}-isobutyl-amine 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:

: [5-(4-Benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pent-(E)-ylidene]-isobutyl-amine

: 869101-66-6
{5-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pentyl}-isobutyl-amine

Guidance literature:: With sodium cyanoborohydride; In methanol; dichloromethane; at 20 ℃;
DOI:10.1016/j.bmc.2005.06.058

Reference yield:

: O,O-di-t-butyloxycarbonylcurcumin

: 869101-66-6
{5-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pentyl}-isobutyl-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: 92.1 percent / H₂ / Pd/C / ethyl acetate / 60 h / 20 °C / 10343 Torr

2.1: trifluoroacetic acid / CH₂Cl₂ / 20 h / 14 °C

2.2: 51.5 percent / H₂ / Pd/C / methanol / 1 h / 20 °C / 760 Torr

3.1: 99 percent / potassium carbonate / dimethylformamide / 0.25 h / microwave irradiation

4.1: HCl / methanol; CH₂Cl₂ / 20 °C

5.1: 233 mg / NaBH₃CN / methanol; CH₂Cl₂ / 20 °C

With hydrogenchloride; hydrogen; sodium cyanoborohydride; potassium carbonate; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.06.058

Reference yield:

: 458-37-7
curcumin

: 869101-66-6
{5-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-pentyl}-isobutyl-amine

Guidance literature:: Multi-step reaction with 6 steps

1.1: 88.7 percent / NaOH / methanol / 3 h / 20 °C

2.1: 92.1 percent / H₂ / Pd/C / ethyl acetate / 60 h / 20 °C / 10343 Torr

3.1: trifluoroacetic acid / CH₂Cl₂ / 20 h / 14 °C

3.2: 51.5 percent / H₂ / Pd/C / methanol / 1 h / 20 °C / 760 Torr

4.1: 99 percent / potassium carbonate / dimethylformamide / 0.25 h / microwave irradiation

5.1: HCl / methanol; CH₂Cl₂ / 20 °C

6.1: 233 mg / NaBH₃CN / methanol; CH₂Cl₂ / 20 °C

With hydrogenchloride; sodium hydroxide; hydrogen; sodium cyanoborohydride; potassium carbonate; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.06.058