methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate

Base Information

Chemical Name:methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate
CAS No.:1338582-42-5
Molecular Formula:C₁₃H₁₂ClFN₂O₂
Molecular Weight:282.702
Hs Code.:

Synonyms:methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate

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Chemical Property of methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate

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Technology Process of methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate

There total 2 articles about methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate 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: 80.0%

: 192701-91-0
methyl 3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate

: 107-04-0
1-Bromo-2-chloroethane

: 1338582-42-5
methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate

Guidance literature:: methyl 3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate; With potassium carbonate; In acetone; for 0.0833333h;

1-Bromo-2-chloroethane; In acetone; at 70 ℃; for 19h;

Reference yield:

: 866588-11-6
3-(4-chlorophenyl)-1H-pyrazole-5-carboxylic acid ethyl ester

: 107-04-0
1-Bromo-2-chloroethane

: 1338582-42-5
methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate

Guidance literature:: With potassium carbonate; In acetone; at 70 ℃; for 4h;

Reference yield: 86.0%

: 1338582-42-5
methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate

: 1338582-43-6
(1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazol-5-yl)methanol

Guidance literature:: methyl 1-(2-chloroethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate; With lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; at 0 ℃; for 2h; Inert atmosphere;

With water; sodium hydroxide; In tetrahydrofuran; diethyl ether; at 0 ℃;