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N-[3-bromo-5-(S)-menthoxy-2(5H)-furanonyl] 4-aminobutyric acid propargyl ester

Base Information
  • Chemical Name:N-[3-bromo-5-(S)-menthoxy-2(5H)-furanonyl] 4-aminobutyric acid propargyl ester
  • CAS No.:1365570-70-2
  • Molecular Formula:C21H30BrNO5
  • Molecular Weight:456.377
  • Hs Code.:
N-[3-bromo-5-(S)-menthoxy-2(5H)-furanonyl] 4-aminobutyric acid propargyl ester

Synonyms:N-[3-bromo-5-(S)-menthoxy-2(5H)-furanonyl] 4-aminobutyric acid propargyl ester

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Chemical Property of N-[3-bromo-5-(S)-menthoxy-2(5H)-furanonyl] 4-aminobutyric acid propargyl ester
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Technology Process of N-[3-bromo-5-(S)-menthoxy-2(5H)-furanonyl] 4-aminobutyric acid propargyl ester

There total 2 articles about N-[3-bromo-5-(S)-menthoxy-2(5H)-furanonyl] 4-aminobutyric acid propargyl 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:
Guidance literature:
C18H28BrNO5; With potassium carbonate; In acetonitrile; for 0.5h; Inert atmosphere;
propargyl bromide; In acetonitrile; at 40 ℃; for 8h; Inert atmosphere;
DOI:10.1007/s11164-011-0429-1
Guidance literature:
Multi-step reaction with 2 steps
1.1: potassium hydroxide / ethanol / 20 °C
2.1: potassium carbonate / acetonitrile / 0.5 h / Inert atmosphere
2.2: 8 h / 40 °C / Inert atmosphere
With potassium carbonate; potassium hydroxide; In ethanol; acetonitrile;
DOI:10.1007/s11164-011-0429-1
upstream raw materials:

C18H28BrNO5

propargyl bromide

C14H20Br2O3

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