1-[6-(4-tert-butyl-cyclohexyloxy)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone

Base Information

Chemical Name:1-[6-(4-tert-butyl-cyclohexyloxy)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone
CAS No.:1266119-96-3
Molecular Formula:C₂₂H₂₅F₃O₂
Molecular Weight:378.435
Hs Code.:

Synonyms:1-[6-(4-tert-butyl-cyclohexyloxy)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone

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Chemical Property of 1-[6-(4-tert-butyl-cyclohexyloxy)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone

Chemical Property:

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Technology Process of 1-[6-(4-tert-butyl-cyclohexyloxy)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone

There total 5 articles about 1-[6-(4-tert-butyl-cyclohexyloxy)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone 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:

: 1225352-09-9
2-bromo-6-(trans-4-tert-butylcyclohexyloxy)naphthalene

: 104863-67-4
N-methoxy-N-methyltrifluoroacetamide

: 1266119-96-3
1-[6-(4-tert-butyl-cyclohexyloxy)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone

Guidance literature:: In tetrahydrofuran; at -78 - 20 ℃; for 2h;

Reference yield:

: 15231-91-1
6-bromo-naphthalen-2-ol

: 1266119-96-3
1-[6-(4-tert-butyl-cyclohexyloxy)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: caesium carbonate / butanone; tert-butyl alcohol / 0.17 h / 110 °C

1.2: 15 h / 110 °C / Inert atmosphere

2.1: tetrahydrofuran / 2 h / -78 - 20 °C

With caesium carbonate; In tetrahydrofuran; butanone; tert-butyl alcohol;

Reference yield:

: 937-05-3
cis-4-tert-butyl-1-cyclohexanol

: 1266119-96-3
1-[6-(4-tert-butyl-cyclohexyloxy)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 3 h / 0 - 20 °C

2: triphenylphosphine; di-isopropyl azodicarboxylate / toluene / 26 h / 0 - 30 °C

3: tetrahydrofuran / 2 h / -78 - 20 °C

With di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; toluene;