(E)-3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}-N-hydroxyacrylamide

Base Information

Chemical Name:(E)-3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}-N-hydroxyacrylamide
CAS No.:1450591-37-3
Molecular Formula:C₂₆H₃₀N₂O₄
Molecular Weight:434.535
Hs Code.:

Synonyms:(E)-3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}-N-hydroxyacrylamide

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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 (E)-3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}-N-hydroxyacrylamide

Chemical Property:

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Technology Process of (E)-3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}-N-hydroxyacrylamide

There total 5 articles about (E)-3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}-N-hydroxyacrylamide 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: 43.3%

: 1450591-00-0
(E)-ethyl 3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}acrylate

: 1450591-37-3
(E)-3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}-N-hydroxyacrylamide

Guidance literature:: With hydroxylamine; potassium hydroxide; In methanol; at 20 ℃; for 1h;
DOI:10.1016/j.bmc.2013.06.009

Reference yield:

: 53282-12-5,53282-26-1
ethyl (E)-3-(2-furyl)prop-2-enoate

: 1450591-37-3
(E)-3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}-N-hydroxyacrylamide

Guidance literature:: Multi-step reaction with 5 steps

1: trichlorophosphate; N,N-dimethyl-formamide / 2.33 h / 0 - 60 °C

2: methanol / 3 h / Reflux

3: sodium tetrahydroborate / methanol / 0.5 h / 20 °C

4: potassium iodide; potassium carbonate / acetonitrile / 8 h / 35 °C

5: hydroxylamine; potassium hydroxide / methanol / 1 h / 20 °C

With sodium tetrahydroborate; hydroxylamine; potassium carbonate; N,N-dimethyl-formamide; potassium iodide; potassium hydroxide; trichlorophosphate; In methanol; acetonitrile;
DOI:10.1016/j.bmc.2013.06.009

Reference yield:

: 191480-39-4
ethyl (E)-3-(5-formylfuran-2-yl)acrylate

: 1450591-37-3
(E)-3-{5-{{benzyl[4-(p-tolyloxy)butyl]amino}methyl}furan-2-yl}-N-hydroxyacrylamide

Guidance literature:: Multi-step reaction with 4 steps

1: methanol / 3 h / Reflux

2: sodium tetrahydroborate / methanol / 0.5 h / 20 °C

3: potassium iodide; potassium carbonate / acetonitrile / 8 h / 35 °C

4: hydroxylamine; potassium hydroxide / methanol / 1 h / 20 °C

With sodium tetrahydroborate; hydroxylamine; potassium carbonate; potassium iodide; potassium hydroxide; In methanol; acetonitrile;
DOI:10.1016/j.bmc.2013.06.009