4-<2-Methyl-1-phenyl-3-(trifluormethylsulfonyloxy)-2-propenyliden>morpholinium-trifluormethansulfonat

Base Information

Chemical Name:4-<2-Methyl-1-phenyl-3-(trifluormethylsulfonyloxy)-2-propenyliden>morpholinium-trifluormethansulfonat
CAS No.:105787-36-8
Molecular Formula:CF₃O₃S*C₁₅H₁₇F₃NO₄S
Molecular Weight:513.436
Hs Code.:

Synonyms:4-<2-Methyl-1-phenyl-3-(trifluormethylsulfonyloxy)-2-propenyliden>morpholinium-trifluormethansulfonat

Suppliers and Price of 4-<2-Methyl-1-phenyl-3-(trifluormethylsulfonyloxy)-2-propenyliden>morpholinium-trifluormethansulfonat

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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 4-<2-Methyl-1-phenyl-3-(trifluormethylsulfonyloxy)-2-propenyliden>morpholinium-trifluormethansulfonat

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Technology Process of 4-<2-Methyl-1-phenyl-3-(trifluormethylsulfonyloxy)-2-propenyliden>morpholinium-trifluormethansulfonat

There total 2 articles about 4-<2-Methyl-1-phenyl-3-(trifluormethylsulfonyloxy)-2-propenyliden>morpholinium-trifluormethansulfonat 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: 85.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 105787-12-0
2-Methyl-3-morpholino-3-phenyl-2-propenal

: 105787-36-8
4-<2-Methyl-1-phenyl-3-(trifluormethylsulfonyloxy)-2-propenyliden>morpholinium-trifluormethansulfonat

Guidance literature:: In dichloromethane; at -40 ℃; for 0.333333h;

Reference yield:

: 31357-82-1
(E)-β-chloro-α-methyl-β-phenylacrolein

: 105787-36-8
4-<2-Methyl-1-phenyl-3-(trifluormethylsulfonyloxy)-2-propenyliden>morpholinium-trifluormethansulfonat

Guidance literature:: Multi-step reaction with 2 steps

1: 40 percent / acetonitrile / 3 h / Heating

2: 85 percent / CH₂Cl₂ / 0.33 h / -40 °C

In dichloromethane; acetonitrile;