1,4-bis[5-(carbethoxy-methyl)-thio-4-(p-ethoxyphenyl)-1,2,4-triazol-3-yl]-butane

Base Information

Chemical Name:1,4-bis[5-(carbethoxy-methyl)-thio-4-(p-ethoxyphenyl)-1,2,4-triazol-3-yl]-butane
CAS No.:1266399-84-1
Molecular Formula:C₃₂H₄₀N₆O₆S₂
Molecular Weight:668.838
Hs Code.:

Synonyms:1,4-bis[5-(carbethoxy-methyl)-thio-4-(p-ethoxyphenyl)-1,2,4-triazol-3-yl]-butane

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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 1,4-bis[5-(carbethoxy-methyl)-thio-4-(p-ethoxyphenyl)-1,2,4-triazol-3-yl]-butane

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Technology Process of 1,4-bis[5-(carbethoxy-methyl)-thio-4-(p-ethoxyphenyl)-1,2,4-triazol-3-yl]-butane

There total 4 articles about 1,4-bis[5-(carbethoxy-methyl)-thio-4-(p-ethoxyphenyl)-1,2,4-triazol-3-yl]-butane 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: 65.0%

: 105-36-2
ethyl bromoacetate

: C₂₄H₂₈N₆O₂S₂

: 1266399-84-1
1,4-bis[5-(carbethoxy-methyl)-thio-4-(p-ethoxyphenyl)-1,2,4-triazol-3-yl]-butane

Guidance literature:: With potassium carbonate; In acetone; for 8h; Reflux;
DOI:10.1007/s00044-010-9517-9

Reference yield:

: 3460-49-9
1-ethoxy-4-isothiocyanatobenzene

: 1266399-84-1
1,4-bis[5-(carbethoxy-methyl)-thio-4-(p-ethoxyphenyl)-1,2,4-triazol-3-yl]-butane

Guidance literature:: Multi-step reaction with 3 steps

1: Reflux

2: Heating; Alkaline conditions

3: acetone / Reflux

In acetone;
DOI:10.1002/ardp.201000177

Reference yield:

: 1071-93-8,98152-55-7
adipic acid dihydrazide

: 1266399-84-1
1,4-bis[5-(carbethoxy-methyl)-thio-4-(p-ethoxyphenyl)-1,2,4-triazol-3-yl]-butane

Guidance literature:: Multi-step reaction with 3 steps

1: Reflux

2: Heating; Alkaline conditions

3: acetone / Reflux

In acetone;
DOI:10.1002/ardp.201000177