(4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone

Base Information

Chemical Name:(4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone
CAS No.:818376-11-3
Molecular Formula:C₂₂H₁₇Cl₄NO₅
Molecular Weight:517.193
Hs Code.:

Synonyms:(4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone

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Chemical Property of (4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone

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Technology Process of (4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone

There total 5 articles about (4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone 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:

: 178043-48-6
3,5-dichloro-4-(3-hydroxypropyloxy)-1-(3,3-dichloro-2-propenyloxy)benzene

: 818376-24-8
3-(4-hydroxybenzoyl)isoxazole

: 818376-11-3
(4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 ℃; for 0.5h;

3,5-dichloro-4-(3-hydroxypropyloxy)-1-(3,3-dichloro-2-propenyloxy)benzene; 3-(4-hydroxybenzoyl)isoxazole; In tetrahydrofuran; at 20 ℃; for 24h;

Reference yield:

: 818376-23-7
3-(4-methoxy-benzoyl)-isoxazole

: 818376-11-3
(4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: boron tribromide / dichloromethane / 72 h / -70 - 20 °C

1.2: 0 °C

2.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0.5 h / 0 °C

2.2: 24 h / 20 °C

With di-isopropyl azodicarboxylate; boron tribromide; triphenylphosphine; In tetrahydrofuran; dichloromethane;

Reference yield:

: 33108-93-9,78335-64-5
α-chloro-α-oximino-p-methoxyacetophenone

: 818376-11-3
(4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydrogencarbonate / isopropyl alcohol / 24 h / 20 °C

2.1: toluene-4-sulfonic acid / toluene / 8 h / Heating / reflux

3.1: boron tribromide / dichloromethane / 72 h / -70 - 20 °C

3.2: 0 °C

4.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0.5 h / 0 °C

4.2: 24 h / 20 °C

With di-isopropyl azodicarboxylate; boron tribromide; sodium hydrogencarbonate; toluene-4-sulfonic acid; triphenylphosphine; In tetrahydrofuran; dichloromethane; isopropyl alcohol; toluene;