tert-butyl (1R,3r,5S)-3-(4-cyanophenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

Base Information

Chemical Name:tert-butyl (1R,3r,5S)-3-(4-cyanophenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate
CAS No.:1267849-02-4
Molecular Formula:C₁₉H₂₄N₂O₃
Molecular Weight:328.411
Hs Code.:

Synonyms:tert-butyl (1R,3r,5S)-3-(4-cyanophenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

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Chemical Property of tert-butyl (1R,3r,5S)-3-(4-cyanophenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

Chemical Property:

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Technology Process of tert-butyl (1R,3r,5S)-3-(4-cyanophenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

There total 4 articles about tert-butyl (1R,3r,5S)-3-(4-cyanophenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate 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:

: 1194-02-1,143234-87-1
4-fluorobenzonitrile

: 143557-91-9
(1R,3S,5S)-tert-butyl 3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate

: 1267849-02-4
tert-butyl (1R,3r,5S)-3-(4-cyanophenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

Guidance literature:: With potassium tert-butylate; In N,N-dimethyl-formamide; at 20 ℃; for 1h;

Reference yield:

: 185099-67-6
N-Boc-nortropinone

: 1267849-02-4
tert-butyl (1R,3r,5S)-3-(4-cyanophenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: calcium chloride / methanol / 0.5 h / Cooling with ice

1.2: 1 h

2.1: potassium tert-butylate / N,N-dimethyl-formamide / 1 h / 20 °C

With potassium tert-butylate; calcium chloride; In methanol; N,N-dimethyl-formamide;

Reference yield:

: (8-azabicyclo[3.2.1]octan-3-one) hydrochloride

: 1267849-02-4
tert-butyl (1R,3r,5S)-3-(4-cyanophenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / water; tetrahydrofuran / 1 h / 20 °C / Cooling with ice

2.1: calcium chloride / methanol / 0.5 h / Cooling with ice

2.2: 1 h

3.1: potassium tert-butylate / N,N-dimethyl-formamide / 1 h / 20 °C

With potassium tert-butylate; calcium chloride; sodium hydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;