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(R)-methyl-1-(4,5-dihydro-4-isopropyl-2-thiazolyl)cyclohexanedithiocarboxylate

Base Information
  • Chemical Name:(R)-methyl-1-(4,5-dihydro-4-isopropyl-2-thiazolyl)cyclohexanedithiocarboxylate
  • CAS No.:420133-89-7
  • Molecular Formula:C14H23NS3
  • Molecular Weight:301.541
  • Hs Code.:
(R)-methyl-1-(4,5-dihydro-4-isopropyl-2-thiazolyl)cyclohexanedithiocarboxylate

Synonyms:(R)-methyl-1-(4,5-dihydro-4-isopropyl-2-thiazolyl)cyclohexanedithiocarboxylate

Suppliers and Price of (R)-methyl-1-(4,5-dihydro-4-isopropyl-2-thiazolyl)cyclohexanedithiocarboxylate
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Chemical Property of (R)-methyl-1-(4,5-dihydro-4-isopropyl-2-thiazolyl)cyclohexanedithiocarboxylate
Chemical Property:
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Technology Process of (R)-methyl-1-(4,5-dihydro-4-isopropyl-2-thiazolyl)cyclohexanedithiocarboxylate

There total 4 articles about (R)-methyl-1-(4,5-dihydro-4-isopropyl-2-thiazolyl)cyclohexanedithiocarboxylate 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:
(R)-2-cyclohexyl-4-isopropyl-2-thiazoline; With tert.-butyl lithium; In tetrahydrofuran; cyclohexane; at -78 ℃; for 3h;
carbon disulfide; In tetrahydrofuran; at -40 ℃; for 2h;
methyl iodide; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/S0957-4166(01)00481-5
Guidance literature:
Multi-step reaction with 3 steps
1.1: 98 percent / Et3N / 48 h / 20 °C
2.1: 98 percent / mesylchloride; Et3N / tetrahydrofuran / 0.17 h / 20 °C
3.1: t-BuLi / tetrahydrofuran; cyclohexane / 3 h / -78 °C
3.2: tetrahydrofuran / 2 h / -40 °C
3.3: 79 percent / tetrahydrofuran / 20 °C
With tert.-butyl lithium; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; cyclohexane;
DOI:10.1016/S0957-4166(01)00481-5
Guidance literature:
Multi-step reaction with 3 steps
1.1: 98 percent / Et3N / 48 h / 20 °C
2.1: 98 percent / mesylchloride; Et3N / tetrahydrofuran / 0.17 h / 20 °C
3.1: t-BuLi / tetrahydrofuran; cyclohexane / 3 h / -78 °C
3.2: tetrahydrofuran / 2 h / -40 °C
3.3: 79 percent / tetrahydrofuran / 20 °C
With tert.-butyl lithium; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; cyclohexane;
DOI:10.1016/S0957-4166(01)00481-5
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