N-[2-(3-fluorophenyl)ethyl]-1,4-dioxaspiro[4.5]decane-6-carboxamide

Base Information

• Chemical Name: N-[2-(3-fluorophenyl)ethyl]-1,4-dioxaspiro[4.5]decane-6-carboxamide
• CAS No.: 854133-17-8
• Molecular Formula: C₁₇H₂₂FNO₃
• Molecular Weight: 307.365
• Mol file: 854133-17-8.mol

Synonyms:N-[2-(3-fluorophenyl)ethyl]-1,4-dioxaspiro[4.5]decane-6-carboxamide

Chemical Property of N-[2-(3-fluorophenyl)ethyl]-1,4-dioxaspiro[4.5]decane-6-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-[2-(3-fluorophenyl)ethyl]-1,4-dioxaspiro[4.5]decane-6-carboxamide

There total 4 articles about N-[2-(3-fluorophenyl)ethyl]-1,4-dioxaspiro[4.5]decane-6-carboxamide 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:

2-(3-Fluorophenyl)ethylamine (404-70-6) + 1,4-dioxa-spiro[4.5]decane-6-carbonyl chloride (854133-07-6) → N-[2-(3-fluorophenyl)ethyl]-1,4-dioxaspiro[4.5]decane-6-carboxamide (854133-17-8)

Guidance literature:

With pyridine; at 20 ℃; for 12h;

DOI:10.1016/j.bmcl.2005.03.054

Reference yield:

1,4-dioxaspiro[4.5]decane-6-carboxylic acid (4746-93-4) → N-[2-(3-fluorophenyl)ethyl]-1,4-dioxaspiro[4.5]decane-6-carboxamide (854133-17-8)

Guidance literature:

Multi-step reaction with 2 steps

1: oxalyl chloride / CH₂Cl₂ / 2 h / 20 °C

2: pyridine / 12 h / 20 °C

With pyridine; oxalyl dichloride; In dichloromethane;

DOI:10.1016/j.bmcl.2005.03.054

Reference yield:

ethyl 1,4-dioxa-spiro[4,5]decane-6-carboxylate (13747-72-3) → N-[2-(3-fluorophenyl)ethyl]-1,4-dioxaspiro[4.5]decane-6-carboxamide (854133-17-8)

Guidance literature:

Multi-step reaction with 3 steps

1: aq. KOH / dioxane / 12 h / 35 °C

2: oxalyl chloride / CH₂Cl₂ / 2 h / 20 °C

3: pyridine / 12 h / 20 °C

With pyridine; potassium hydroxide; oxalyl dichloride; In 1,4-dioxane; dichloromethane;

DOI:10.1016/j.bmcl.2005.03.054

upstream raw materials:

2-(3-Fluorophenyl)ethylamine

1,4-dioxa-spiro[4.5]decane-6-carbonyl chloride

1,4-dioxaspiro[4.5]decane-6-carboxylic acid

ethyl 1,4-dioxa-spiro[4,5]decane-6-carboxylate

Downstream raw materials:

acetic acid 2-{2-[2-(3-fluoro-phenyl)-ethylcarbamoyl]-cyclohex-1-enylcarbamoyl}-phenyl ester

2-amino-N-[2-(3-fluorophenyl)ethyl]-1-cyclohexene-1-carboxamide

N-[2-(3-fluorophenyl)ethyl]-2-oxocyclohexanecarboxamide