c-4-p-chlorobenzoyloxy-3-p-chlorophenyl-r-3-cyano-4,5-dihydro-3H-pyrazole

Base Information

Chemical Name:c-4-p-chlorobenzoyloxy-3-p-chlorophenyl-r-3-cyano-4,5-dihydro-3H-pyrazole
CAS No.:135641-65-5
Molecular Formula:C₁₇H₁₁Cl₂N₃O₂
Molecular Weight:360.199
Hs Code.:

Synonyms:c-4-p-chlorobenzoyloxy-3-p-chlorophenyl-r-3-cyano-4,5-dihydro-3H-pyrazole

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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 c-4-p-chlorobenzoyloxy-3-p-chlorophenyl-r-3-cyano-4,5-dihydro-3H-pyrazole

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Technology Process of c-4-p-chlorobenzoyloxy-3-p-chlorophenyl-r-3-cyano-4,5-dihydro-3H-pyrazole

There total 3 articles about c-4-p-chlorobenzoyloxy-3-p-chlorophenyl-r-3-cyano-4,5-dihydro-3H-pyrazole 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: 86.0%

: 186581-53-3,908094-01-9,334-88-3
diazomethane

: 135641-64-4
(Z)-β-p-chlorobenzoyloxy-α-cyano-p-chlorostyrene

: 135641-65-5
c-4-p-chlorobenzoyloxy-3-p-chlorophenyl-r-3-cyano-4,5-dihydro-3H-pyrazole

Guidance literature:: In diethyl ether; dichloromethane; for 24h; Ambient temperature;

Reference yield:

: 122-01-0
4-chloro-benzoyl chloride

: 135641-65-5
c-4-p-chlorobenzoyloxy-3-p-chlorophenyl-r-3-cyano-4,5-dihydro-3H-pyrazole

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) RT, 1 d

2: 86 percent / CH₂Cl₂; diethyl ether / 24 h / Ambient temperature

With triethylamine; In diethyl ether; dichloromethane;

Reference yield:

: 53283-56-0
3-hydroxy-2-(p-chlorophenyl)propenenitrile

: 135641-65-5
c-4-p-chlorobenzoyloxy-3-p-chlorophenyl-r-3-cyano-4,5-dihydro-3H-pyrazole

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) RT, 1 d

2: 86 percent / CH₂Cl₂; diethyl ether / 24 h / Ambient temperature

With triethylamine; In diethyl ether; dichloromethane;