(1S)-1-(adamantan-1-yl)ethan-1-amine hydrochloride

Base Information

• Chemical Name: (1S)-1-(adamantan-1-yl)ethan-1-amine hydrochloride
• CAS No.: 1005341-54-7
• Molecular Formula: C₁₂H₂₁N*ClH
• Molecular Weight: 215.766

Synonyms:(1S)-1-(adamantan-1-yl)ethan-1-amine hydrochloride;1005341-54-7;(1S)-1-(1-adamantyl)ethanamine;hydrochloride;Rimantadine (Flumadine);AKOS026675604;PS-7934;(1S)-1-(Adamantan-1-yl)ethan-1-amine HCl;EN300-119256;G23347;(S)-1-(Adamantan-1-yl)ethan-1-aminehydrochloride;(S)-1-(Adamantan-1-yl)ethan-1-amine hydrochloride

Chemical Property of (1S)-1-(adamantan-1-yl)ethan-1-amine hydrochloride

Chemical Property:

• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 215.1440774
• Heavy Atom Count: 14
• Complexity: 180

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(C12CC3CC(C1)CC(C3)C2)N.Cl
• Isomeric SMILES: C[C@@H](C12CC3CC(C1)CC(C3)C2)N.Cl

Technology Process of (1S)-1-(adamantan-1-yl)ethan-1-amine hydrochloride

There total 3 articles about (1S)-1-(adamantan-1-yl)ethan-1-amine 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:

Reference yield: 95.0%

N-[1-(1’-adamantyl)ethyl]isopropylsulfinamide → (S)-N-[1-(1’-adamantyl)ethyl]amine hydrochloride (1005341-54-7)

Guidance literature:

With hydrogenchloride; at 0 - 20 ℃; Inert atmosphere;

DOI:10.1039/c9ob02241d

Reference yield:

(R)-N-[1-(1’-adamantyl)ethylidene]isopropylsulfinylimine → (S)-N-[1-(1’-adamantyl)ethyl]amine hydrochloride (1005341-54-7)

Guidance literature:

Multi-step reaction with 2 steps

1: L-Selectride / tetrahydrofuran / 24 h / -78 - -40 °C / Inert atmosphere

2: hydrogenchloride / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; L-Selectride; In tetrahydrofuran;

DOI:10.1039/c9ob02241d

Reference yield:

1-acetyladamantane (1660-04-4) → (S)-N-[1-(1’-adamantyl)ethyl]amine hydrochloride (1005341-54-7)

Guidance literature:

Multi-step reaction with 3 steps

1: titanium(IV) tetraethanolate / tetrahydrofuran / 24 h / 70 °C / Inert atmosphere

2: L-Selectride / tetrahydrofuran / 24 h / -78 - -40 °C / Inert atmosphere

3: hydrogenchloride / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; titanium(IV) tetraethanolate; L-Selectride; In tetrahydrofuran;

DOI:10.1039/c9ob02241d

upstream raw materials:

1-acetyladamantane

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