ethyl 4-(2,2-dimethyl-4-trifluorosulfonyloxy-(2H)-chromen-6-ylethynyl)-benzoate

Base Information

Chemical Name:ethyl 4-(2,2-dimethyl-4-trifluorosulfonyloxy-(2H)-chromen-6-ylethynyl)-benzoate
CAS No.:229961-62-0
Molecular Formula:C₂₃H₁₉F₃O₆S
Molecular Weight:480.461
Hs Code.:

Synonyms:ethyl 4-(2,2-dimethyl-4-trifluorosulfonyloxy-(2H)-chromen-6-ylethynyl)-benzoate

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Chemical Property of ethyl 4-(2,2-dimethyl-4-trifluorosulfonyloxy-(2H)-chromen-6-ylethynyl)-benzoate

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Technology Process of ethyl 4-(2,2-dimethyl-4-trifluorosulfonyloxy-(2H)-chromen-6-ylethynyl)-benzoate

There total 8 articles about ethyl 4-(2,2-dimethyl-4-trifluorosulfonyloxy-(2H)-chromen-6-ylethynyl)-benzoate 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:

: 2-[N,N-bis(trifluoromethanesulfonyl)amino]-5-pyridine

aqueous NH₄ Cl: aqueous NH₄ Cl

: 229961-61-9
ethyl 4-<(2,2-dimethyl-4-oxo-chroman-6-yl)ethynyl>benzoate

: 229961-62-0
ethyl 4-(2,2-dimethyl-4-trifluorosulfonyloxy-(2H)-chromen-6-ylethynyl)-benzoate

Guidance literature:: With sodium hexamethyldisilazane; In tetrahydrofuran;

Reference yield:

: 99853-21-1
6-bromo-2,2-dimethylchroman-4-one

: 229961-62-0
ethyl 4-(2,2-dimethyl-4-trifluorosulfonyloxy-(2H)-chromen-6-ylethynyl)-benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / CuI, Et₃N / Pd(PPh₃)2Cl₂ / 624 h / 70 °C

2: 91 percent / K₂CO₃ / methanol / 24 h / Ambient temperature

3: 50 percent / Et₃N, CuI / Pd(PPh₃)2Cl₂ / Ambient temperature

4: 1.) NaN(TMS)2 / 1.) THF, -78 deg C, 30 min, 2.) THF, room temperature, overnight

With copper(l) iodide; sodium hexamethyldisilazane; potassium carbonate; triethylamine; bis-triphenylphosphine-palladium(II) chloride; In methanol;
DOI:10.1016/S0968-0896(99)00055-3

Reference yield:

: 106-41-2
4-bromo-phenol

: 229961-62-0
ethyl 4-(2,2-dimethyl-4-trifluorosulfonyloxy-(2H)-chromen-6-ylethynyl)-benzoate

Guidance literature:: Multi-step reaction with 7 steps

1: 83 percent / Et₃N / CH₂Cl₂ / 21 h / Ambient temperature

2: 72 percent / AlCl₃ / 0.5 h / 150 °C

3: 62 percent / piperidine, TFA / benzene / 43 h / Heating

4: 89 percent / CuI, Et₃N / Pd(PPh₃)2Cl₂ / 624 h / 70 °C

5: 91 percent / K₂CO₃ / methanol / 24 h / Ambient temperature

6: 50 percent / Et₃N, CuI / Pd(PPh₃)2Cl₂ / Ambient temperature

7: 1.) NaN(TMS)2 / 1.) THF, -78 deg C, 30 min, 2.) THF, room temperature, overnight

With piperidine; copper(l) iodide; aluminium trichloride; sodium hexamethyldisilazane; potassium carbonate; triethylamine; trifluoroacetic acid; bis-triphenylphosphine-palladium(II) chloride; In methanol; dichloromethane; benzene;
DOI:10.1016/S0968-0896(99)00055-3