Q₃FA₁₈

Base Information

Chemical Name:Q₃FA₁₈
CAS No.:887604-32-2
Molecular Formula:C₂₇H₄₈O₄
Molecular Weight:436.676
Hs Code.:

Synonyms:Q₃FA₁₈

Suppliers and Price of Q₃FA₁₈

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Q₃FA₁₈

Chemical Property:

Purity/Quality:

Safty Information:

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Technology Process of Q₃FA₁₈

There total 8 articles about Q₃FA₁₈ 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:

: 59101-28-9
16-bromohexadecan-1-ol

: 887604-32-2
Q₃FA₁₈

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaH / tetrahydrofuran / 0.5 h / 20 °C

1.2: tetrahydrofuran / 24 h / Heating

2.1: dimethylsulfoxide / 0 - 20 °C

3.1: piperidine; Pd(PPh₃)4 / 24 h / 80 °C

4.1: H₂ / Pd/C / ethanol / 20 °C

With piperidine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; hydrogen; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; ethanol; dimethyl sulfoxide; 3.1: Sonogashira cross-coupling;
DOI:10.1016/j.bmcl.2006.02.041

Reference yield:

: 887604-17-3
1-(18-Benzyloxy-octadec-1-ynyl)-2,4,5-trimethoxy-benzene

: 887604-32-2
Q₃FA₁₈

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; at 20 ℃;
DOI:10.1016/j.bmcl.2006.02.041

Reference yield:

: 887604-07-1
octadec-17-ynyloxymethyl-benzene

: 887604-32-2
Q₃FA₁₈

Guidance literature:: Multi-step reaction with 2 steps

1: piperidine; Pd(PPh₃)4 / 24 h / 80 °C

2: H₂ / Pd/C / ethanol / 20 °C

With piperidine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; hydrogen; palladium on activated charcoal; In ethanol; 1: Sonogashira cross-coupling;
DOI:10.1016/j.bmcl.2006.02.041