C₁₆H₃₀O

Base Information

Chemical Name:C₁₆H₃₀O
CAS No.:1393360-35-4
Molecular Formula:C₁₆H₃₀O
Molecular Weight:238.414
Hs Code.:

Synonyms:C₁₆H₃₀O

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₁₆H₃₀O

Chemical Property:

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Technology Process of C₁₆H₃₀O

There total 4 articles about C₁₆H₃₀O 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: 50.0%

: 1073-13-8
4,4-dimethylcyclohexenone

: 14850-23-8
trans-4-Octene

: 1393360-35-4
C₁₆H₃₀O

Guidance literature:: trans-4-Octene; With Schwartz's reagent; In tetrahydrofuran; dichloromethane; at 60 ℃;

4,4-dimethylcyclohexenone; With chloro-trimethyl-silane; silver trifluoromethanesulfonate; copper(l) chloride; (3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)-bis-(1-phenyl-ethyl)-amine; In diethyl ether;
DOI:10.1071/CH14556

Reference yield:

: 1073-13-8
4,4-dimethylcyclohexenone

: 111-66-0,25068-25-1
oct-1-ene

: 1393360-35-4
C₁₆H₃₀O

: C₁₆H₃₀O

Guidance literature:: oct-1-ene; With Schwartz's reagent; In dichloromethane; at 20 ℃;

4,4-dimethylcyclohexenone; With chloro-trimethyl-silane; C₃₆H₃₀NO₂P*Cu⁽¹⁺⁾*CF₃O₃S^(1-); In diethyl ether; at 20 ℃; Concentration; Overall yield = 49 %; Optical yield = 89 %ee; enantioselective reaction;

Reference yield:

: 1073-13-8
4,4-dimethylcyclohexenone

: 592-99-4,7642-15-1,14850-23-8
4-octene

: 1393360-35-4
C₁₆H₃₀O

: C₁₆H₃₀O

Guidance literature:: 4-octene; With Schwartz's reagent; In dichloromethane; at 20 ℃;

4,4-dimethylcyclohexenone; With chloro-trimethyl-silane; C₃₆H₃₀NO₂P*Cu⁽¹⁺⁾*CF₃O₃S^(1-); In diethyl ether; at 20 ℃; Concentration; Overall yield = 36 %; Optical yield = 78 %ee; enantioselective reaction;