trifluoro-methanesulfonic acid 2-formyl-3-methoxymethyl-5-(tetrahydro-pyran-2-yloxy)-phenyl ester

Base Information

Chemical Name:trifluoro-methanesulfonic acid 2-formyl-3-methoxymethyl-5-(tetrahydro-pyran-2-yloxy)-phenyl ester
CAS No.:1265359-59-8
Molecular Formula:C₁₅H₁₇F₃O₇S
Molecular Weight:398.357
Hs Code.:

Synonyms:trifluoro-methanesulfonic acid 2-formyl-3-methoxymethyl-5-(tetrahydro-pyran-2-yloxy)-phenyl ester

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Chemical Property of trifluoro-methanesulfonic acid 2-formyl-3-methoxymethyl-5-(tetrahydro-pyran-2-yloxy)-phenyl ester

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Technology Process of trifluoro-methanesulfonic acid 2-formyl-3-methoxymethyl-5-(tetrahydro-pyran-2-yloxy)-phenyl ester

There total 9 articles about trifluoro-methanesulfonic acid 2-formyl-3-methoxymethyl-5-(tetrahydro-pyran-2-yloxy)-phenyl ester 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: 72.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 1265359-57-6
2-hydroxy-6-methoxymethyl-4-(tetrahydro-pyran-2-yloxy)-benzaldehyde

: 1265359-59-8
trifluoro-methanesulfonic acid 2-formyl-3-methoxymethyl-5-(tetrahydro-pyran-2-yloxy)-phenyl ester

Guidance literature:: With triethylamine; In dichloromethane; at -78 ℃; for 1h;

Reference yield:

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 1265359-59-8
trifluoro-methanesulfonic acid 2-formyl-3-methoxymethyl-5-(tetrahydro-pyran-2-yloxy)-phenyl ester

Guidance literature:: Multi-step reaction with 8 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1.5 h / 0 - 20 °C

2.1: lithium aluminium tetrahydride / diethyl ether / 1 h / 0 - 20 °C

3.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 0.5 h / 20 °C

4.1: sodium hydride / tetrahydrofuran; mineral oil / 0.33 h / 0 - 20 °C

4.2: 2 h / 20 °C

5.1: n-butyllithium / diethyl ether; hexane / 1 h / -78 °C

5.2: 3 h / 20 °C

6.1: hydrogenchloride / tetrahydrofuran; water / 20 h / 20 °C

7.1: pyridinium p-toluenesulfonate / dichloromethane / 16 h / 20 °C

8.1: triethylamine / dichloromethane / 1 h / -78 °C

With hydrogenchloride; N-Bromosuccinimide; lithium aluminium tetrahydride; n-butyllithium; sodium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; pyridinium p-toluenesulfonate; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 110-87-2
3,4-dihydro-2H-pyran

: 1265359-59-8
trifluoro-methanesulfonic acid 2-formyl-3-methoxymethyl-5-(tetrahydro-pyran-2-yloxy)-phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: pyridinium p-toluenesulfonate / dichloromethane / 16 h / 20 °C

2: triethylamine / dichloromethane / 1 h / -78 °C

With triethylamine; pyridinium p-toluenesulfonate; In dichloromethane;