[1-hydroxymethyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl ester

Base Information

• Chemical Name: [1-hydroxymethyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl ester
• CAS No.: 1309459-64-0
• Molecular Formula: C₁₆H₂₄N₂O₅
• Molecular Weight: 324.377
• Mol file: 1309459-64-0.mol

Synonyms:[1-hydroxymethyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl ester

Chemical Property of [1-hydroxymethyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [1-hydroxymethyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl ester

There total 6 articles about [1-hydroxymethyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl 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: 92.0%

2-Amino-5-(4-nitrophenyl)-pentan-1-ol (1142811-85-5) + 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile (58632-95-4) → [1-hydroxymethyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl ester (1309459-64-0)

Guidance literature:

In acetonitrile; at 20 ℃; for 4.33333h;

DOI:10.1039/c0cc05707j

Reference yield:

2-amino-5-(4-nitrophenyl)pentanoic acid (1206716-20-2) → [1-hydroxymethyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl ester (1309459-64-0)

Guidance literature:

Multi-step reaction with 4 steps

1: hydrogenchloride / 0 - 20 °C

2: triethylamine / methanol; diethyl ether / 1 h / -10 °C

3: sodium tetrahydroborate / methanol / 0 - 20 °C

4: acetonitrile / 4.33 h / 20 °C

With hydrogenchloride; sodium tetrahydroborate; triethylamine; In methanol; diethyl ether; acetonitrile;

DOI:10.1039/c0cc05707j

Reference yield:

1-bromo-3-(4-nitrophenyl)propane (53712-77-9) → [1-hydroxymethyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl ester (1309459-64-0)

Guidance literature:

Multi-step reaction with 5 steps

1.1: sodium ethanolate / ethanol / 1.67 h / 50 °C / Reflux

1.2: 108 h / Reflux

1.3: 24 h / Reflux

2.1: hydrogenchloride / 0 - 20 °C

3.1: triethylamine / methanol; diethyl ether / 1 h / -10 °C

4.1: sodium tetrahydroborate / methanol / 0 - 20 °C

5.1: acetonitrile / 4.33 h / 20 °C

With hydrogenchloride; sodium tetrahydroborate; sodium ethanolate; triethylamine; In methanol; diethyl ether; ethanol; acetonitrile;

DOI:10.1039/c0cc05707j

upstream raw materials:

2-Amino-5-(4-nitrophenyl)-pentan-1-ol

2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile

2-amino-5-(4-nitrophenyl)pentanoic acid methyl ester

2-amino-5-(4-nitrophenyl)pentanoic acid

Downstream raw materials:

3p-C-NETA

[1-formyl-4-(4-nitrophenyl)butyl]carbamic acid tert-butyl ester

7-[2-tert-butoxycarbonylamino-5-(4-nitrophenyl)pentyl]-[1,4,7]triazonane-1,4-dicarboxylic acid di-tert-butyl ester

4-(4-nitrophenyl)-1-[1,4,7]triazonan-1-ylmethyl-butylamine