N-Benzyltetrahydrofuran-3-amine

Base Information

• Chemical Name: N-Benzyltetrahydrofuran-3-amine
• CAS No.: 162851-40-3
• Molecular Formula: C₁₁H₁₅NO
• Molecular Weight: 177.246
• Hs Code.: 2932190090
• European Community (EC) Number: 962-563-7
• DSSTox Substance ID: DTXSID80566396
• Mol file: 162851-40-3.mol

Synonyms:N-Benzyltetrahydrofuran-3-amine;162851-40-3;N-benzyloxolan-3-amine;N-BENZYL-TETRAHYDROFURAN-3-AMINE;3-Furanamine, tetrahydro-N-(phenylmethyl)-;SCHEMBL3937405;DTXSID80566396;AKOS012636104;EN300-265435;F1906-0105;Z1124552713

Chemical Property of N-Benzyltetrahydrofuran-3-amine

Chemical Property:

• PSA: 21.26000
• LogP: 1.95600
• XLogP3: 1.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 177.115364102
• Heavy Atom Count: 13
• Complexity: 143

Purity/Quality:

99% ^*data from raw suppliers

N-benzyltetrahydrofuran-3-amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1COCC1NCC2=CC=CC=C2

Technology Process of N-Benzyltetrahydrofuran-3-amine

There total 1 articles about N-Benzyltetrahydrofuran-3-amine 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:

→ N-benzyltetrahydrofuran-3-amine (162851-40-3)

Guidance literature:

With magnesium sulfate; In dichloromethane; at 25 ℃; for 12h;

With sodium tetrahydroborate; In methanol; at 25 ℃; for 5h;

Reference yield:

N-benzyltetrahydrofuran-3-amine (162851-40-3) → N-benzyl-2-{5-[(methylcarbamoyl)amino]-3’,5’-dioxo-2,3-dihydrospiro[indene-1,2'-[1,4]oxazolidine]-4’-yl}-N-(oxolan-3-yl)acetamide

Guidance literature:

Multi-step reaction with 4 steps

1.1: dichloromethane / 2 h / 0 - 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 20 °C

3.1: hydrogenchloride / water; methanol / 2 h / Reflux

4.1: triethylamine / dichloromethane / 1.5 h / 0 - 20 °C

4.2: 0.5 h / 20 °C

With hydrogenchloride; potassium carbonate; triethylamine; In methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

N-benzyltetrahydrofuran-3-amine (162851-40-3) → 2-(5-acetamido-2',4'-dioxo-2,3-dihydrospiro[indene-1,5'-oxazolidine]-3'-yl)-N-benzyl-N-(tetrahydrofuran-3-yl)acetamide

Guidance literature:

Multi-step reaction with 2 steps

1: dichloromethane / 2 h / 0 - 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 1 h / 20 °C

With potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;

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