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(2R,6R)-1-Benzyl-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-6-pentyl-piperidine-2-carbaldehyde

Base Information
  • Chemical Name:(2R,6R)-1-Benzyl-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-6-pentyl-piperidine-2-carbaldehyde
  • CAS No.:122624-23-1
  • Molecular Formula:C24H37NO3
  • Molecular Weight:387.563
  • Hs Code.:
(2R,6R)-1-Benzyl-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-6-pentyl-piperidine-2-carbaldehyde

Synonyms:(2R,6R)-1-Benzyl-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-6-pentyl-piperidine-2-carbaldehyde

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Chemical Property of (2R,6R)-1-Benzyl-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-6-pentyl-piperidine-2-carbaldehyde
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Technology Process of (2R,6R)-1-Benzyl-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-6-pentyl-piperidine-2-carbaldehyde

There total 12 articles about (2R,6R)-1-Benzyl-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-6-pentyl-piperidine-2-carbaldehyde 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:
Multi-step reaction with 12 steps
1: 71 percent / hydroxylamine-O-sulfonic acid, formic acid / 1 h / Heating
2: 1.) t-BuOK / 1.) THF, RT, 10 min, 2.) THF, reflux, 1 h
3: 95 percent / Lawesson's reagent / hexamethylphosphoric acid triamide / 2.5 h / 100 °C
5: 2.) triethylamine / 1.) 65-70 deg C, 3 h, 2.) dichloromethane, RT, 1 h
6: 98 percent / Raney nickel W2 / acetone / 4 h / Heating
7: 1.) bromine, 2.) water, triethylamine / 1.) ether, dichloromethane, -70 deg C, 1.5 h, 2.) RT, 2 h
8: 59 percent / toluene / 40 h / 110 °C
9: H2, KOH / 5percent Pd/C / ethyl acetate; ethanol / 0.58 h / Ambient temperature
10: 82 percent / p-toluenesulfonic acid / toluene / 6 h / Heating
11: Dibal / diethyl ether; toluene / 6 h / -78 °C
12: oxalyl chloride, dimethyl sulfoxide / CH2Cl2 / 0.5 h / -60 °C
With Lawessons reagent; potassium hydroxide; formic acid; oxalyl dichloride; potassium tert-butylate; water; hydrogen; bromine; diisobutylaluminium hydride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; hydroxylamine-O-sulfonic acid; palladium on activated charcoal; Raney nickel W2; In N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; ethanol; dichloromethane; ethyl acetate; acetone; toluene;
DOI:10.1021/jo00279a034
Guidance literature:
Multi-step reaction with 11 steps
1: 1.) t-BuOK / 1.) THF, RT, 10 min, 2.) THF, reflux, 1 h
2: 95 percent / Lawesson's reagent / hexamethylphosphoric acid triamide / 2.5 h / 100 °C
4: 2.) triethylamine / 1.) 65-70 deg C, 3 h, 2.) dichloromethane, RT, 1 h
5: 98 percent / Raney nickel W2 / acetone / 4 h / Heating
6: 1.) bromine, 2.) water, triethylamine / 1.) ether, dichloromethane, -70 deg C, 1.5 h, 2.) RT, 2 h
7: 59 percent / toluene / 40 h / 110 °C
8: H2, KOH / 5percent Pd/C / ethyl acetate; ethanol / 0.58 h / Ambient temperature
9: 82 percent / p-toluenesulfonic acid / toluene / 6 h / Heating
10: Dibal / diethyl ether; toluene / 6 h / -78 °C
11: oxalyl chloride, dimethyl sulfoxide / CH2Cl2 / 0.5 h / -60 °C
With Lawessons reagent; potassium hydroxide; oxalyl dichloride; potassium tert-butylate; water; hydrogen; bromine; diisobutylaluminium hydride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; palladium on activated charcoal; Raney nickel W2; In N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; ethanol; dichloromethane; ethyl acetate; acetone; toluene;
DOI:10.1021/jo00279a034
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