2-methyl-4-oxo-3-pentyl-cyclopent-2-enecarboxylic acid ethyl ester

Base Information

Chemical Name:2-methyl-4-oxo-3-pentyl-cyclopent-2-enecarboxylic acid ethyl ester
CAS No.:96934-07-5
Molecular Formula:C₁₄H₂₂O₃
Molecular Weight:238.327
Hs Code.:

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Chemical Property of 2-methyl-4-oxo-3-pentyl-cyclopent-2-enecarboxylic acid ethyl ester

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Technology Process of 2-methyl-4-oxo-3-pentyl-cyclopent-2-enecarboxylic acid ethyl ester

There total 3 articles about 2-methyl-4-oxo-3-pentyl-cyclopent-2-enecarboxylic acid ethyl 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:

: 111-13-7
hexyl-methyl-ketone

: 123-25-1
succinic acid diethyl ester

: 96934-07-5
2-methyl-4-oxo-3-pentyl-cyclopent-2-enecarboxylic acid ethyl ester

Guidance literature:: With potassium tert-butylate; aufeinanderfolgende Umsetzung des hierbei erhaltenen Monoaethylesters mit SOCl₂ und mit SnCl₄;
DOI:10.1039/jr9560002231

Reference yield:

: 111-13-7
hexyl-methyl-ketone

: 123-25-1
succinic acid diethyl ester

: 91765-45-6
((Ξ)-1-methyl-heptylidene)-succinic acid-anhydride

: 96934-07-5
2-methyl-4-oxo-3-pentyl-cyclopent-2-enecarboxylic acid ethyl ester

Guidance literature:: With potassium tert-butylate; tert-butyl alcohol; Behandeln des Reaktionsprodukts mit Thionylchlorid, Pyridin und Benzol und Behandeln der Reaktionsloesung mit Zinn(IV)-chlorid;
DOI:10.1039/jr9560002231

Reference yield:

: 96934-07-5
2-methyl-4-oxo-3-pentyl-cyclopent-2-enecarboxylic acid ethyl ester

Guidance literature:: Methyl-hexyl-keton, 1.) Bernsteinsaeureaethylester, Natriumhydrid, Bzl.; 2.) wss. Eg.; 3.) Bzl., Thionylchlorid, Py.; 4.) SnCl2; 5.) SiO2;
DOI:10.1002/hlca.19620450234