2-Phenyl-4-(16-phenyl-hexadecyloxymethyl)-4,5-dihydro-oxazole

Base Information

• Chemical Name: 2-Phenyl-4-(16-phenyl-hexadecyloxymethyl)-4,5-dihydro-oxazole
• CAS No.: 151312-90-2
• Molecular Formula: C₃₂H₄₇NO₂
• Molecular Weight: 477.731
• Mol file: 151312-90-2.mol

Synonyms:2-Phenyl-4-(16-phenyl-hexadecyloxymethyl)-4,5-dihydro-oxazole

Chemical Property of 2-Phenyl-4-(16-phenyl-hexadecyloxymethyl)-4,5-dihydro-oxazole

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

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Technology Process of 2-Phenyl-4-(16-phenyl-hexadecyloxymethyl)-4,5-dihydro-oxazole

There total 1 articles about 2-Phenyl-4-(16-phenyl-hexadecyloxymethyl)-4,5-dihydro-oxazole 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-phenyl-4,5-dihydrooxazol-4-yl)methanol (15263-48-6) + 1-bromo-16-phenylhexadecane → 2-Phenyl-4-(16-phenyl-hexadecyloxymethyl)-4,5-dihydro-oxazole (151312-90-2)

Guidance literature:

With potassium hydride; Yield given. Multistep reaction; 1.) benzene, RT, 30 min, 2.) benzene, RT, 18 h;

DOI:10.1080/00397919308011175

Reference yield: 82.0%

2-Phenyl-4-(16-phenyl-hexadecyloxymethyl)-4,5-dihydro-oxazole (151312-90-2) → (S)-2-Amino-3-(16-phenyl-hexadecyloxy)-propan-1-ol (154093-85-3)

Guidance literature:

With hydrogenchloride; In ethanol; for 24h; Heating;

DOI:10.1080/00397919308011175

Reference yield:

2-Phenyl-4-(16-phenyl-hexadecyloxymethyl)-4,5-dihydro-oxazole (151312-90-2) → Hexadecanoic acid [(S)-1-hydroxymethyl-2-(16-phenyl-hexadecyloxy)-ethyl]-amide (154093-87-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 82 percent / 4 M aq. HCl / ethanol / 24 h / Heating

2: 88 percent / DMAP / CHCl₃ / 1.5 h / 0 °C

With hydrogenchloride; dmap; In ethanol; chloroform;

DOI:10.1080/00397919308011175

upstream raw materials:

(2-phenyl-4,5-dihydrooxazol-4-yl)methanol

Downstream raw materials:

(S)-2-Amino-3-(16-phenyl-hexadecyloxy)-propan-1-ol

Hexadecanoic acid [(S)-1-hydroxymethyl-2-(16-phenyl-hexadecyloxy)-ethyl]-amide

(S)-3-(16-Phenyl-hexadecyloxy)-2-(trityl-amino)-propan-1-ol

Phosphoric acid 2-bromo-ethyl ester (R)-3-(16-phenyl-hexadecyloxy)-2-(trityl-amino)-propyl ester