phenyl cyclopentanecarboxylate

Base Information

Chemical Name:phenyl cyclopentanecarboxylate
CAS No.:54758-32-6
Molecular Formula:C₁₂H₁₄O₂
Molecular Weight:190.242
Hs Code.:

Synonyms:phenyl cyclopentanecarboxylate

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Chemical Property of phenyl cyclopentanecarboxylate

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Technology Process of phenyl cyclopentanecarboxylate

There total 6 articles about phenyl cyclopentanecarboxylate 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%

: (1H-benzo[d][1,2,3]triazol-1-yl)(cyclopentyl)methanone

: 108-95-2,27073-41-2
phenol

: 54758-32-6
phenyl cyclopentanecarboxylate

Guidance literature:: With triethylamine; at 50 ℃; for 1h; Microwave irradiation;
DOI:10.1002/chem.201403529

Reference yield:

: 3400-45-1
cyclopentanecarboxylic acid

: 88284-48-4
2-(trimethylsilyl)phenyl trifluoromethanesulfonate

: 51795-96-1
cyclopentyl-(2-hydroxy-phenyl)-methanone

: 54758-32-6
phenyl cyclopentanecarboxylate

Guidance literature:: cyclopentanecarboxylic acid; 2-(trimethylsilyl)phenyl trifluoromethanesulfonate; With sodium hydroxide; In acetonitrile; at 20 ℃; for 0.166667h; Inert atmosphere;

With cesium fluoride; In acetonitrile; at 80 ℃; for 4h; Overall yield = 48 %; chemoselective reaction; Inert atmosphere;
DOI:10.1016/j.tetlet.2015.08.019

Reference yield:

: 201230-82-2
carbon monoxide

: 1556-18-9
cyclopentyl iodide

: 108-95-2,27073-41-2
phenol

: 54758-32-6
phenyl cyclopentanecarboxylate

Guidance literature:: With rhodium(III) chloride; 1,3-bis-(diphenylphosphino)propane; sodium carbonate; sodium bromide; In 1,4-dioxane; at 120 ℃; for 24h; under 750.075 Torr; chemoselective reaction; Inert atmosphere;
DOI:10.1021/acscatal.0c00933