(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester

Base Information

Chemical Name:(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester
CAS No.:120476-76-8
Molecular Formula:C₁₉H₂₈Cl₂N₂O₅
Molecular Weight:435.348
Hs Code.:

Synonyms:(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester

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Chemical Property of (8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester

Chemical Property:

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Technology Process of (8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester

There total 5 articles about (8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl 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: 70.0%

: 120476-67-7
N-(3-chloropropyl)-8-chloro-6-hydroxyoctylamine

: 4457-32-3
4-nitrobenzyl chloroformate

: 120476-76-8
(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester

Guidance literature:: With potassium hydroxide; In diethyl ether; Ambient temperature;
DOI:10.1021/jm00126a026

Reference yield:

: 1070-65-1
6-hydroxy-8-chlorooctanoic acid ethyl ester

: 120476-76-8
(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: LiOH*H₂O / aq. ethanol / Ambient temperature

2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature

3: 75.4 percent / B₂H₆ / tetrahydrofuran / Ambient temperature

4: 70 percent / 1M KOH / diethyl ether / Ambient temperature

With 4-methyl-morpholine; potassium hydroxide; lithium hydroxide; benzotriazol-1-ol; dicyclohexyl-carbodiimide; diborane; In tetrahydrofuran; diethyl ether; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00126a026

Reference yield:

: 90435-60-2
(+)-8-chloro-6-hydroxy-octanoic acid

: 120476-76-8
(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature

2: 75.4 percent / B₂H₆ / tetrahydrofuran / Ambient temperature

3: 70 percent / 1M KOH / diethyl ether / Ambient temperature

With 4-methyl-morpholine; potassium hydroxide; benzotriazol-1-ol; dicyclohexyl-carbodiimide; diborane; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1021/jm00126a026