(Z)-3-[3-(3-chlorophenyl)-[1,2,4]-triazol-1-yl]acrylic acid tert-butyl ester

Base Information

Chemical Name:(Z)-3-[3-(3-chlorophenyl)-[1,2,4]-triazol-1-yl]acrylic acid tert-butyl ester
CAS No.:1333151-68-0
Molecular Formula:C₁₅H₁₆ClN₃O₂
Molecular Weight:305.764
Hs Code.:

Synonyms:(Z)-3-[3-(3-chlorophenyl)-[1,2,4]-triazol-1-yl]acrylic acid tert-butyl ester

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Chemical Property of (Z)-3-[3-(3-chlorophenyl)-[1,2,4]-triazol-1-yl]acrylic acid tert-butyl ester

Chemical Property:

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Technology Process of (Z)-3-[3-(3-chlorophenyl)-[1,2,4]-triazol-1-yl]acrylic acid tert-butyl ester

There total 5 articles about (Z)-3-[3-(3-chlorophenyl)-[1,2,4]-triazol-1-yl]acrylic acid tert-butyl ester 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:

: 13831-03-3
tert-butyl prop-2-ynoate

: 52853-74-4
3-(3-chlorophenyl)-1,2,4-triazole

: 1333151-68-0
(Z)-3-[3-(3-chlorophenyl)-[1,2,4]-triazol-1-yl]acrylic acid tert-butyl ester

: 1333152-25-2
C₁₅H₁₆ClN₃O₂

Guidance literature:: With triethylamine; In acetonitrile; at 20 ℃; Heating; Inert atmosphere;

Reference yield:

: 764621-09-2
C₈H₈ClNS

: 1333151-68-0
(Z)-3-[3-(3-chlorophenyl)-[1,2,4]-triazol-1-yl]acrylic acid tert-butyl ester

: 1333152-25-2
C₁₅H₁₆ClN₃O₂

Guidance literature:: Multi-step reaction with 2 steps

1: N,N-dimethyl-formamide / 90 °C / Inert atmosphere

2: triethylamine / acetonitrile / 20 °C / Heating; Inert atmosphere

With triethylamine; In N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 766-84-7
3-chloro-benzonitrile

: 1333151-68-0
(Z)-3-[3-(3-chlorophenyl)-[1,2,4]-triazol-1-yl]acrylic acid tert-butyl ester

: 1333152-25-2
C₁₅H₁₆ClN₃O₂

Guidance literature:: Multi-step reaction with 4 steps

1: magnesium(II) chloride hexahydrate; sodium monohydrogen sulfide x-hydrate / N,N-dimethyl-formamide / 2 h / 20 °C

2: diethyl ether / 24 h

3: N,N-dimethyl-formamide / 90 °C / Inert atmosphere

4: triethylamine / acetonitrile / 20 °C / Heating; Inert atmosphere

With sodium monohydrogen sulfide x-hydrate; magnesium(II) chloride hexahydrate; triethylamine; In diethyl ether; N,N-dimethyl-formamide; acetonitrile;