Technology Process of 1-chloro-3,3-dimethylcyclobutyl p-tolylsulfoxide
There total 8 articles about 1-chloro-3,3-dimethylcyclobutyl p-tolylsulfoxide which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
N-chloro-succinimide;
In
tetrahydrofuran;
at 0 - 20 ℃;
for 5h;
DOI:10.1055/s-0031-1291011
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 3-chloro-benzenecarboperoxoic acid / chloroform / 5 h / -50 - 15 °C
2: sodium tetrahydroborate / tetrahydrofuran; methanol / 2.5 h / 0 °C / Reflux
3: triethylamine / tetrahydrofuran / 2.08 h / -78 - -15 °C
4: sodium tetrahydroborate / 1,3-dimethyl-2-imidazolidinone / 1.5 h / 0 - 100 °C
5: N-chloro-succinimide / tetrahydrofuran / 5 h / 0 - 20 °C
With
sodium tetrahydroborate; N-chloro-succinimide; triethylamine; 3-chloro-benzenecarboperoxoic acid;
In
tetrahydrofuran; 1,3-dimethyl-2-imidazolidinone; methanol; chloroform;
DOI:10.1055/s-0031-1291011
- Guidance literature:
-
Multi-step reaction with 8 steps
1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 12 h / 20 °C / 760.05 Torr
2: dmap; triethylamine / chloroform / 3.5 h / 0 °C
3: potassium tert-butylate / tert-butyl alcohol / 15 h / Reflux
4: 3-chloro-benzenecarboperoxoic acid / chloroform / 5 h / -50 - 15 °C
5: sodium tetrahydroborate / tetrahydrofuran; methanol / 2.5 h / 0 °C / Reflux
6: triethylamine / tetrahydrofuran / 2.08 h / -78 - -15 °C
7: sodium tetrahydroborate / 1,3-dimethyl-2-imidazolidinone / 1.5 h / 0 - 100 °C
8: N-chloro-succinimide / tetrahydrofuran / 5 h / 0 - 20 °C
With
dmap; sodium tetrahydroborate; N-chloro-succinimide; palladium 10% on activated carbon; potassium tert-butylate; hydrogen; triethylamine; 3-chloro-benzenecarboperoxoic acid;
In
tetrahydrofuran; 1,3-dimethyl-2-imidazolidinone; methanol; chloroform; ethyl acetate; tert-butyl alcohol;
DOI:10.1055/s-0031-1291011