3,4,5-tridodecyloxy-benzoic acid 6-(3-tert-butoxycarbonylmethyl-ureido)-hexyl ester

Base Information

Chemical Name:3,4,5-tridodecyloxy-benzoic acid 6-(3-tert-butoxycarbonylmethyl-ureido)-hexyl ester
CAS No.:336884-82-3
Molecular Formula:C₅₆H₁₀₂N₂O₈
Molecular Weight:931.434
Hs Code.:

Synonyms:3,4,5-tridodecyloxy-benzoic acid 6-(3-tert-butoxycarbonylmethyl-ureido)-hexyl ester

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Chemical Property of 3,4,5-tridodecyloxy-benzoic acid 6-(3-tert-butoxycarbonylmethyl-ureido)-hexyl ester

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Technology Process of 3,4,5-tridodecyloxy-benzoic acid 6-(3-tert-butoxycarbonylmethyl-ureido)-hexyl ester

There total 4 articles about 3,4,5-tridodecyloxy-benzoic acid 6-(3-tert-butoxycarbonylmethyl-ureido)-hexyl 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: 76.0%

: 117241-31-3
3,4,5-tridodecyloxy benzoic acid

: 336884-81-2
[3-(6-hydroxy-hexyl)-ureido]-acetic acid tert-butyl ester

: 336884-82-3
3,4,5-tridodecyloxy-benzoic acid 6-(3-tert-butoxycarbonylmethyl-ureido)-hexyl ester

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In chloroform; at 0 - 20 ℃; for 48h;
DOI:10.1021/jo001573x

Reference yield:

: 4048-33-3
6-amino-1-hexanol

: 336884-82-3
3,4,5-tridodecyloxy-benzoic acid 6-(3-tert-butoxycarbonylmethyl-ureido)-hexyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: CHCl₃ / 0.33 h / 20 °C

2: 4.2 g / CHCl₃ / 20 °C

3: 76 percent / DMAP; DCC / CHCl₃ / 48 h / 0 - 20 °C

With dmap; dicyclohexyl-carbodiimide; In chloroform;
DOI:10.1021/jo001573x

Reference yield:

: 6456-74-2
Glycine tert-butyl ester

: 336884-82-3
3,4,5-tridodecyloxy-benzoic acid 6-(3-tert-butoxycarbonylmethyl-ureido)-hexyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 4.2 g / CHCl₃ / 20 °C

2: 76 percent / DMAP; DCC / CHCl₃ / 48 h / 0 - 20 °C

With dmap; dicyclohexyl-carbodiimide; In chloroform;
DOI:10.1021/jo001573x