2-(3-[benzyl-(4-hydroxy-butyl)-amino]-1-{2-[benzyl-(4-hydroxy-butyl)-amino]-ethyl}-propyl)-malonic acid diethyl ester

Base Information

• Chemical Name: 2-(3-[benzyl-(4-hydroxy-butyl)-amino]-1-{2-[benzyl-(4-hydroxy-butyl)-amino]-ethyl}-propyl)-malonic acid diethyl ester
• CAS No.: 1026133-38-9
• Molecular Formula: C₃₄H₅₂N₂O₆
• Molecular Weight: 584.797
• Mol file: 1026133-38-9.mol

Synonyms:2-(3-[benzyl-(4-hydroxy-butyl)-amino]-1-{2-[benzyl-(4-hydroxy-butyl)-amino]-ethyl}-propyl)-malonic acid diethyl ester

Chemical Property of 2-(3-[benzyl-(4-hydroxy-butyl)-amino]-1-{2-[benzyl-(4-hydroxy-butyl)-amino]-ethyl}-propyl)-malonic acid diethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-(3-[benzyl-(4-hydroxy-butyl)-amino]-1-{2-[benzyl-(4-hydroxy-butyl)-amino]-ethyl}-propyl)-malonic acid diethyl ester

There total 4 articles about 2-(3-[benzyl-(4-hydroxy-butyl)-amino]-1-{2-[benzyl-(4-hydroxy-butyl)-amino]-ethyl}-propyl)-malonic acid diethyl ester 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:

4-iodo-1,6-heptadiene (921926-33-2) → 2-(3-[benzyl-(4-hydroxy-butyl)-amino]-1-{2-[benzyl-(4-hydroxy-butyl)-amino]-ethyl}-propyl)-malonic acid diethyl ester (1026133-38-9)

Guidance literature:

Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran / 0 - 20 °C

1.2: 94.8 percent / tetrahydrofuran / 120 h / Heating

2.1: 99.6 percent / bis(tricyclohexylphosphine)benzylidine ruthenium dichloride / CH₂Cl₂ / 2 h

3.1: ozone / ethyl acetate / -78 °C

3.2: H₂ / Pd/C / ethyl acetate / 0.08 h / 20 °C / 1551.44 Torr

4.1: NaBH(OAc)3 / 1,2-dichloro-ethane / 0 - 20 °C

With sodium tris(acetoxy)borohydride; sodium hydride; ozone; Grubbs catalyst first generation; In tetrahydrofuran; dichloromethane; ethyl acetate; 1,2-dichloro-ethane;

DOI:10.1021/jo0617262

Reference yield:

diethyl 2-(4-(1,6-heptadiene)) malonate (921926-37-6) → 2-(3-[benzyl-(4-hydroxy-butyl)-amino]-1-{2-[benzyl-(4-hydroxy-butyl)-amino]-ethyl}-propyl)-malonic acid diethyl ester (1026133-38-9)

Guidance literature:

Multi-step reaction with 3 steps

1.1: 99.6 percent / bis(tricyclohexylphosphine)benzylidine ruthenium dichloride / CH₂Cl₂ / 2 h

2.1: ozone / ethyl acetate / -78 °C

2.2: H₂ / Pd/C / ethyl acetate / 0.08 h / 20 °C / 1551.44 Torr

3.1: NaBH(OAc)3 / 1,2-dichloro-ethane / 0 - 20 °C

With sodium tris(acetoxy)borohydride; ozone; Grubbs catalyst first generation; In dichloromethane; ethyl acetate; 1,2-dichloro-ethane;

DOI:10.1021/jo0617262

Reference yield:

1, 6-heptadien-4-ol (2883-45-6) → 2-(3-[benzyl-(4-hydroxy-butyl)-amino]-1-{2-[benzyl-(4-hydroxy-butyl)-amino]-ethyl}-propyl)-malonic acid diethyl ester (1026133-38-9)

Guidance literature:

Multi-step reaction with 5 steps

1.1: 76.3 percent / triphenylphosphine; imidazole; iodine / CH₂Cl₂ / 6 h / 20 °C

2.1: sodium hydride / tetrahydrofuran / 0 - 20 °C

2.2: 94.8 percent / tetrahydrofuran / 120 h / Heating

3.1: 99.6 percent / bis(tricyclohexylphosphine)benzylidine ruthenium dichloride / CH₂Cl₂ / 2 h

4.1: ozone / ethyl acetate / -78 °C

4.2: H₂ / Pd/C / ethyl acetate / 0.08 h / 20 °C / 1551.44 Torr

5.1: NaBH(OAc)3 / 1,2-dichloro-ethane / 0 - 20 °C

With 1H-imidazole; iodine; sodium tris(acetoxy)borohydride; sodium hydride; ozone; triphenylphosphine; Grubbs catalyst first generation; In tetrahydrofuran; dichloromethane; ethyl acetate; 1,2-dichloro-ethane;

DOI:10.1021/jo0617262

upstream raw materials:

4-iodo-1,6-heptadiene

diethyl 2-(4-(1,6-heptadiene)) malonate

1, 6-heptadien-4-ol

Cyclopent-3-en-1-yl-malonsaeurediethylester