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(R)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxylmethyl)phenylmethacrylate mandelate

Base Information Edit
  • Chemical Name:(R)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxylmethyl)phenylmethacrylate mandelate
  • CAS No.:1390644-38-8
  • Molecular Formula:C8H8O3*C26H35NO3
  • Molecular Weight:561.719
  • Hs Code.:
  • Mol file:1390644-38-8.mol
(R)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxylmethyl)phenylmethacrylate mandelate

Synonyms:(R)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxylmethyl)phenylmethacrylate mandelate

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Chemical Property of (R)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxylmethyl)phenylmethacrylate mandelate Edit
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Technology Process of (R)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxylmethyl)phenylmethacrylate mandelate

There total 23 articles about (R)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxylmethyl)phenylmethacrylate mandelate 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:
Guidance literature:
PNU 200577 l-mandelate salt; With sodium carbonate; In chloroform; water; at 0 - 5 ℃; for 0.25h;
Methacryloyl chloride; With potassium carbonate; In chloroform; at -45 - -35 ℃; for 0.75h;
With (S)-Mandelic acid; In ethyl acetate; at 0 - 50 ℃;
Guidance literature:
Multi-step reaction with 7 steps
1.1: sulfuric acid; acetic acid / 16 h / 100 °C
2.1: acetone / 2 h / 25 - 35 °C
3.1: boron trifluoride diethyl etherate / tetrahydrofuran / 1 h / -20 °C
4.1: hydrogen / 5%-palladium/activated carbon / methanol / 18 h / 25 - 35 °C / 2942.29 Torr / autoclave
5.1: potassium carbonate / acetone / 6 h / Reflux
6.1: isopropyl alcohol / 0.5 h / Reflux
7.1: sodium carbonate / chloroform; water / 0.25 h / 0 - 5 °C
7.2: 0.75 h / -45 - -35 °C
7.3: 0 - 50 °C
With sulfuric acid; boron trifluoride diethyl etherate; hydrogen; sodium carbonate; potassium carbonate; acetic acid; 5%-palladium/activated carbon; In tetrahydrofuran; methanol; chloroform; water; isopropyl alcohol; acetone;
Guidance literature:
Multi-step reaction with 9 steps
1.1: dmap; triethylamine / dichloromethane / 2 h / 0 - 5 °C
2.1: acetonitrile / 32 h / 95 - 100 °C / autoclave; Inert atmosphere
3.1: isopropyl alcohol / 30 - 55 °C
4.1: sodium hydroxide; water / dichloromethane / 0.25 h / 10 - 20 °C / pH 11.5
4.2: 4 h / 25 - 55 °C / Inert atmosphere
4.3: -70 - -10 °C / Inert atmosphere
5.1: thionyl chloride / 5 h / 40 - 45 °C
6.1: sodium bis(2-methoxyethoxy)aluminium dihydride / toluene / 4 h / 0 - 5 °C / Inert atmosphere
7.1: hydrogen / 5%-palladium/activated carbon / methanol / 8 h / 25 - 30 °C / 2206.72 - 2942.29 Torr
8.1: isopropyl alcohol / 0.5 h / Reflux
9.1: sodium carbonate / chloroform; water / 0.25 h / 0 - 5 °C
9.2: 0.75 h / -45 - -35 °C
9.3: 0 - 50 °C
With dmap; thionyl chloride; water; hydrogen; sodium carbonate; triethylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; sodium hydroxide; 5%-palladium/activated carbon; In methanol; dichloromethane; chloroform; water; isopropyl alcohol; toluene; acetonitrile;
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