Technology Process of C18H24O4
There total 7 articles about C18H24O4 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:
- Guidance literature:
-
With
camphor-10-sulfonic acid;
In
acetonitrile;
DOI:10.1021/ol402017x
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 5 - 8 h / 110 °C
1.2: 48 h / 20 °C
2.1: tetrahydrofuran / 3 h / -80 °C
3.1: 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran; isopropyl alcohol / 75 °C
4.1: camphor-10-sulfonic acid / acetonitrile
With
camphor-10-sulfonic acid; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
tetrahydrofuran; isopropyl alcohol; acetonitrile;
3.1: |Stetter 1,4-Dicarbonyl Synthesis;
DOI:10.1021/ol402017x
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: diisobutylaluminium hydride / tetrahydrofuran; n-heptane / 5 h / 20 °C
1.2: 20 °C
2.1: tetrahydrofuran; diethyl ether / 5 h / -40 °C
3.1: 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran; isopropyl alcohol / 75 °C
4.1: camphor-10-sulfonic acid / acetonitrile
With
camphor-10-sulfonic acid; diisobutylaluminium hydride; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
tetrahydrofuran; diethyl ether; n-heptane; isopropyl alcohol; acetonitrile;
3.1: |Stetter 1,4-Dicarbonyl Synthesis;
DOI:10.1021/ol402017x
