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(1R,2R,4R)-2-(4-bromophenyl)-4-morpholin-4-ylcyclohexanecarboxylic acid hydrochloride

Base Information Edit
  • Chemical Name:(1R,2R,4R)-2-(4-bromophenyl)-4-morpholin-4-ylcyclohexanecarboxylic acid hydrochloride
  • CAS No.:1350711-82-8
  • Molecular Formula:C17H22BrNO3*ClH
  • Molecular Weight:404.732
  • Hs Code.:
  • Mol file:1350711-82-8.mol
(1R,2R,4R)-2-(4-bromophenyl)-4-morpholin-4-ylcyclohexanecarboxylic acid hydrochloride

Synonyms:(1R,2R,4R)-2-(4-bromophenyl)-4-morpholin-4-ylcyclohexanecarboxylic acid hydrochloride

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Chemical Property of (1R,2R,4R)-2-(4-bromophenyl)-4-morpholin-4-ylcyclohexanecarboxylic acid hydrochloride Edit
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Technology Process of (1R,2R,4R)-2-(4-bromophenyl)-4-morpholin-4-ylcyclohexanecarboxylic acid hydrochloride

There total 9 articles about (1R,2R,4R)-2-(4-bromophenyl)-4-morpholin-4-ylcyclohexanecarboxylic acid hydrochloride 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:
methyl (1R,2R,4R)-2-(4-bromophenyl)-4-morpholin-4-ylcyclohexanecarboxylate; With lithium hydroxide; In tetrahydrofuran; at 70 ℃; for 24h;
With hydrogenchloride; In water; acetone; Cooling with ice;
Guidance literature:
Multi-step reaction with 8 steps
1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 5 h / 20 °C
2.1: n-butyllithium / tetrahydrofuran / 0.58 h / -65 °C
2.2: 0.75 h / -65 °C
3.1: diethylaluminium chloride / dichloromethane / 0 - 20 °C
4.1: 2,2-Dimethyl-1,3-propanediol / toluene-4-sulfonic acid / toluene / 3 h / Reflux
4.2: 0 - 20 °C
5.1: sodium hydrogen sulfate / water; ethyl acetate / 12 h / 20 °C
6.1: methanol / benzene / 20 °C
7.1: titanium(IV) isopropylate / dichloromethane / 20 °C
7.2: -78 - 20 °C
8.1: lithium hydroxide / tetrahydrofuran / 24 h / 70 °C
8.2: Cooling with ice
With titanium(IV) isopropylate; methanol; sodium hydrogen sulfate; n-butyllithium; oxalyl dichloride; diethylaluminium chloride; 2,2-Dimethyl-1,3-propanediol; lithium hydroxide; toluene-4-sulfonic acid; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane; water; ethyl acetate; toluene; benzene;
Guidance literature:
Multi-step reaction with 5 steps
1.1: 2,2-Dimethyl-1,3-propanediol / toluene-4-sulfonic acid / toluene / 3 h / Reflux
1.2: 0 - 20 °C
2.1: sodium hydrogen sulfate / water; ethyl acetate / 12 h / 20 °C
3.1: methanol / benzene / 20 °C
4.1: titanium(IV) isopropylate / dichloromethane / 20 °C
4.2: -78 - 20 °C
5.1: lithium hydroxide / tetrahydrofuran / 24 h / 70 °C
5.2: Cooling with ice
With titanium(IV) isopropylate; methanol; sodium hydrogen sulfate; 2,2-Dimethyl-1,3-propanediol; lithium hydroxide; toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; water; ethyl acetate; toluene; benzene;
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