methylthio-methyl-n-propylphenylphosphonium trifluoromethanesulfonate

Base Information

Chemical Name:methylthio-methyl-n-propylphenylphosphonium trifluoromethanesulfonate
CAS No.:72315-67-4
Molecular Formula:CF₃O₃S*C₁₁H₁₈PS
Molecular Weight:362.374
Hs Code.:

Synonyms:

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Chemical Property of methylthio-methyl-n-propylphenylphosphonium trifluoromethanesulfonate

Chemical Property:

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Technology Process of methylthio-methyl-n-propylphenylphosphonium trifluoromethanesulfonate

There total 4 articles about methylthio-methyl-n-propylphenylphosphonium trifluoromethanesulfonate 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:

: 87152-18-9
(+)R-methyl-n-propylphenylmethylselenophosphonium triflate

: 72315-67-4,87174-00-3
methylthio-methyl-n-propylphenylphosphonium trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / NaSH / diethyl ether / -75 °C

2: CH₂Cl₂

With sodium hydrogensulfide; In diethyl ether; dichloromethane;
DOI:10.1016/S0040-4020(01)81908-6

Reference yield:

: 34641-79-7
(+)R-methyl-n-propylphenylphosphine selenide

: 72315-67-4,87174-00-3
methylthio-methyl-n-propylphenylphosphonium trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: CH₂Cl₂

2: 62 percent / NaSH / diethyl ether / -75 °C

3: CH₂Cl₂

With sodium hydrogensulfide; In diethyl ether; dichloromethane;
DOI:10.1016/S0040-4020(01)81908-6

Reference yield:

: 33995-97-0
(+)-(R)-methyl-n-propylphenylphosphine selenide

: 72315-67-4,87174-00-3
methylthio-methyl-n-propylphenylphosphonium trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: CH₂Cl₂

2: sodium hydrogen sulphide / methanol

3: CH₂Cl₂

With sodium hydrogensulfide; In methanol; dichloromethane;