methyl {(2S,4R)-1-[(1S)-4-methyl-1-(4,4,4-trifluorobutyl)pent-4-en-2-yn-1-yl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetate

Base Information

Chemical Name:methyl {(2S,4R)-1-[(1S)-4-methyl-1-(4,4,4-trifluorobutyl)pent-4-en-2-yn-1-yl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetate
CAS No.:956466-05-0
Molecular Formula:C₂₅H₂₉F₆NO₂
Molecular Weight:489.501
Hs Code.:

Synonyms:methyl {(2S,4R)-1-[(1S)-4-methyl-1-(4,4,4-trifluorobutyl)pent-4-en-2-yn-1-yl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetate

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Chemical Property of methyl {(2S,4R)-1-[(1S)-4-methyl-1-(4,4,4-trifluorobutyl)pent-4-en-2-yn-1-yl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetate

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Technology Process of methyl {(2S,4R)-1-[(1S)-4-methyl-1-(4,4,4-trifluorobutyl)pent-4-en-2-yn-1-yl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetate

There total 5 articles about methyl {(2S,4R)-1-[(1S)-4-methyl-1-(4,4,4-trifluorobutyl)pent-4-en-2-yn-1-yl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetate 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: 76.0%

: 884602-78-2
(+)-methyl {(2S,4R)-2-[4-(trifluoromethyl)phenyl]-4-piperidinyl}acetate

: 250253-47-5
5,5,5-trifluoropentanal

: 78-80-8
2-methylbut-1-en-3-yne

: 956466-05-0
methyl {(2S,4R)-1-[(1S)-4-methyl-1-(4,4,4-trifluorobutyl)pent-4-en-2-yn-1-yl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetate

Guidance literature:: With gold(III) tribromide; In water; at 70 ℃; for 0.333333h; Microwave irradiation;

Reference yield:

: 884600-79-7
methyl {2-[4-(trifluoromethyl)phenyl]-4-pyridinyl}acetate

: 956466-05-0
methyl {(2S,4R)-1-[(1S)-4-methyl-1-(4,4,4-trifluorobutyl)pent-4-en-2-yn-1-yl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride; hydrogen / platinum(IV) oxide / methanol / 5 h / 1034.32 Torr

2.1: water; sodium hydrogencarbonate

3.1: isopropyl alcohol / 20 °C

3.2: 2 h

4.1: water; sodium carbonate

5.1: gold(III) tribromide / water / 0.33 h / 70 °C / Microwave irradiation

With hydrogenchloride; gold(III) tribromide; water; hydrogen; sodium hydrogencarbonate; sodium carbonate; platinum(IV) oxide; In methanol; water; isopropyl alcohol;

Reference yield:

: 89866-61-5
5,5,5-Trifluorovaleronitrile

: 956466-05-0
methyl {(2S,4R)-1-[(1S)-4-methyl-1-(4,4,4-trifluorobutyl)pent-4-en-2-yn-1-yl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetate

Guidance literature:: Multi-step reaction with 2 steps

1: diisobutylaluminium hydride / dichloromethane; toluene / 1.5 h / -78 °C

2: gold(III) tribromide / water / 0.33 h / 70 °C / Microwave irradiation

With gold(III) tribromide; diisobutylaluminium hydride; In dichloromethane; water; toluene;