1-[1-(Acetylamino)ethyl]naphthalen-2-yl acetate

Base Information

• Chemical Name: 1-[1-(Acetylamino)ethyl]naphthalen-2-yl acetate
• CAS No.: 6640-35-3
• Molecular Formula: C₁₆H₁₇NO₃
• Molecular Weight: 271.316
• NSC Number: 48863
• DSSTox Substance ID: DTXSID20287078
• Mol file: 6640-35-3.mol

Synonyms:6640-35-3;1-(1-Acetamidoethyl)naphthalen-2-yl acetate;1-[1-(acetylamino)ethyl]naphthalen-2-yl acetate;NSC48863;DTXSID20287078;NSC-48863

Chemical Property of 1-[1-(Acetylamino)ethyl]naphthalen-2-yl acetate

Chemical Property:

• Vapor Pressure: 2.53E-09mmHg at 25°C
• Boiling Point: 478.7°C at 760 mmHg
• Flash Point: 243.3°C
• Density: 1.16g/cm³
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 271.12084340
• Heavy Atom Count: 20
• Complexity: 369

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C1=C(C=CC2=CC=CC=C21)OC(=O)C)NC(=O)C

Technology Process of 1-[1-(Acetylamino)ethyl]naphthalen-2-yl acetate

There total 3 articles about 1-[1-(Acetylamino)ethyl]naphthalen-2-yl acetate 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:

1,3-dimethyl-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazine (6296-72-6) → 2-acetoxy-1-(1-acetylamino-ethyl)-naphthalene (6640-35-3)

Guidance literature:

Multi-step reaction with 2 steps

1: aqueous HCl; isopropyl alcohol

2: pyridine; diethyl ether

With pyridine; hydrogenchloride; diethyl ether; isopropyl alcohol;

DOI:10.1021/ja01634a027

Reference yield:

β-naphthol (135-19-3) → 2-acetoxy-1-(1-acetylamino-ethyl)-naphthalene (6640-35-3)

Guidance literature:

Multi-step reaction with 3 steps

1: benzene

2: aqueous HCl; isopropyl alcohol

3: pyridine; diethyl ether

With pyridine; hydrogenchloride; diethyl ether; isopropyl alcohol; benzene;

DOI:10.1021/ja01634a027

Reference yield:

1-(1-amino-ethyl)-[2]naphthol (802271-19-8) + acetic anhydride (108-24-7) → 2-acetoxy-1-(1-acetylamino-ethyl)-naphthalene (6640-35-3)

Guidance literature:

With pyridine; diethyl ether;

DOI:10.1021/ja01634a027

upstream raw materials:

1-(1-amino-ethyl)-[2]naphthol

acetic anhydride

1,3-dimethyl-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazine

β-naphthol