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trans-3-[(S)-hydroxy(pyridin-2-yl)methyl]-1-methyl-3-[4-(trifluoromethoxy)phenyl]cyclobutanol hydrochloride

Base Information
  • Chemical Name:trans-3-[(S)-hydroxy(pyridin-2-yl)methyl]-1-methyl-3-[4-(trifluoromethoxy)phenyl]cyclobutanol hydrochloride
  • CAS No.:1432050-00-4
  • Molecular Formula:C18H18F3NO3*ClH
  • Molecular Weight:389.802
  • Hs Code.:
trans-3-[(S)-hydroxy(pyridin-2-yl)methyl]-1-methyl-3-[4-(trifluoromethoxy)phenyl]cyclobutanol hydrochloride

Synonyms:trans-3-[(S)-hydroxy(pyridin-2-yl)methyl]-1-methyl-3-[4-(trifluoromethoxy)phenyl]cyclobutanol hydrochloride

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Chemical Property of trans-3-[(S)-hydroxy(pyridin-2-yl)methyl]-1-methyl-3-[4-(trifluoromethoxy)phenyl]cyclobutanol hydrochloride
Chemical Property:
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Technology Process of trans-3-[(S)-hydroxy(pyridin-2-yl)methyl]-1-methyl-3-[4-(trifluoromethoxy)phenyl]cyclobutanol hydrochloride

There total 11 articles about trans-3-[(S)-hydroxy(pyridin-2-yl)methyl]-1-methyl-3-[4-(trifluoromethoxy)phenyl]cyclobutanol hydrochloride 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:
Guidance literature:
Multi-step reaction with 6 steps
1.1: sodium t-butanolate / dimethyl sulfoxide; water / 20 - 125 °C
2.1: methanol / 20 - 70 °C
3.1: n-butyllithium / hexane; diethyl ether / 0.67 h / -78 °C
3.2: -78 - 20 °C
4.1: formic acid; triethylamine; (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II) / 192 h / 55 °C
5.1: diethyl ether; tetrahydrofuran / 0 °C / Cooling with acetone-dry ice
6.1: hydrogenchloride / methanol
With hydrogenchloride; methanol; (1S,2S)-(+)-N-tosyl-1,2-diphenylethane-1,2-diamine[η6-1-isopropyl-4-methylbenzene]-ruthenium(II); n-butyllithium; formic acid; triethylamine; sodium t-butanolate; In tetrahydrofuran; methanol; diethyl ether; hexane; water; dimethyl sulfoxide;
Guidance literature:
Multi-step reaction with 7 steps
1.1: toluene-4-sulfonic acid / toluene / 1.5 h / Reflux
1.2: 20 - 100 °C
2.1: n-butyllithium / hexane; diethyl ether / 0.75 h / Cooling with acetone-dry ice
2.2: 20 °C
3.1: methanol; sodium tetrahydroborate / 20 °C
4.1: hydrogenchloride / water; acetone / 20 °C
5.1: Chiralpak AD DAC column / Resolution of racemate
6.1: diethyl ether; tetrahydrofuran / 0 °C / Cooling with acetone-dry ice
7.1: hydrogenchloride / methanol
With hydrogenchloride; methanol; sodium tetrahydroborate; n-butyllithium; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; diethyl ether; hexane; water; acetone; toluene;
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