[1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexyl]-phosphonic acid diethyl ester

Base Information

• Chemical Name: [1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexyl]-phosphonic acid diethyl ester
• CAS No.: 107503-23-1
• Molecular Formula: C₁₉H₃₀NO₄P
• Molecular Weight: 367.425
• Mol file: 107503-23-1.mol

Synonyms:[1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexyl]-phosphonic acid diethyl ester

Chemical Property of [1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexyl]-phosphonic acid diethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexyl]-phosphonic acid diethyl ester

There total 5 articles about [1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexyl]-phosphonic acid diethyl ester 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: 72.0%

amyl iodide (628-17-1) + (5-Phenyl-4,5-dihydro-isoxazol-3-ylmethyl)-phosphonic acid diethyl ester (107487-00-3) → [1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexyl]-phosphonic acid diethyl ester (107503-23-1)

Guidance literature:

With n-butyllithium; In tetrahydrofuran; hexane; -78 deg C, 1 h, 0 deg C, 1 h, RT, 11 h;

DOI:10.1246/bcsj.60.2463

Reference yield:

(2-oxoethyl)phosphonic acid diethyl ester (1606-75-3) → [1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexyl]-phosphonic acid diethyl ester (107503-23-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 95 percent / aq. hydroxylamine hydrochloride / ethanol / 11.5 h / Ambient temperature

2: 1.) NBS; 2.) triethylamine / 1.) DMF, -20 deg C, 1 h, 0 deg C, 30 min; 2.) DMF, Et₂O, RT, 18 h

3: 72 percent / 1.6 M n-BuLi / hexane; tetrahydrofuran / -78 deg C, 1 h, 0 deg C, 1 h, RT, 11 h

With N-Bromosuccinimide; n-butyllithium; hydroxylamine hydrochloride; triethylamine; In tetrahydrofuran; ethanol; hexane;

DOI:10.1246/bcsj.60.2463

Reference yield:

N-<2-(diethoxyphosphoryl)ethylidene>hydroxylamine (110841-50-4) → [1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexyl]-phosphonic acid diethyl ester (107503-23-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) NBS; 2.) triethylamine / 1.) DMF, -20 deg C, 1 h, 0 deg C, 30 min; 2.) DMF, Et₂O, RT, 18 h

2: 72 percent / 1.6 M n-BuLi / hexane; tetrahydrofuran / -78 deg C, 1 h, 0 deg C, 1 h, RT, 11 h

With N-Bromosuccinimide; n-butyllithium; triethylamine; In tetrahydrofuran; hexane;

DOI:10.1246/bcsj.60.2463

upstream raw materials:

amyl iodide

(5-Phenyl-4,5-dihydro-isoxazol-3-ylmethyl)-phosphonic acid diethyl ester

styrene

(2-oxoethyl)phosphonic acid diethyl ester

Downstream raw materials:

1-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-hexan-1-one