3β-benzoyloxy-8-(2-(3,5-dihydroxyphenyl)-2-oxoethyl)-8-azabicyclo[3.2.1]octane

Base Information

Chemical Name:3β-benzoyloxy-8-(2-(3,5-dihydroxyphenyl)-2-oxoethyl)-8-azabicyclo[3.2.1]octane
CAS No.:1360460-74-7
Molecular Formula:C₂₂H₂₃NO₅
Molecular Weight:381.428
Hs Code.:

Synonyms:3β-benzoyloxy-8-(2-(3,5-dihydroxyphenyl)-2-oxoethyl)-8-azabicyclo[3.2.1]octane

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Chemical Property of 3β-benzoyloxy-8-(2-(3,5-dihydroxyphenyl)-2-oxoethyl)-8-azabicyclo[3.2.1]octane

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Technology Process of 3β-benzoyloxy-8-(2-(3,5-dihydroxyphenyl)-2-oxoethyl)-8-azabicyclo[3.2.1]octane

There total 5 articles about 3β-benzoyloxy-8-(2-(3,5-dihydroxyphenyl)-2-oxoethyl)-8-azabicyclo[3.2.1]octane 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:

: 532-24-1
tropinone

: 1360460-74-7
3β-benzoyloxy-8-(2-(3,5-dihydroxyphenyl)-2-oxoethyl)-8-azabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 5 steps

1: aluminum isopropoxide / isopropyl alcohol / 24.75 h / Reflux

2: triethylamine / toluene / 4 h / Reflux

3: 1,2-dichloro-ethane / 19 h / Cooling with ice; Inert atmosphere; Reflux

4: methanol / 22 h / 20 °C / Reflux

5: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 °C

With aluminum isopropoxide; triethylamine; N-ethyl-N,N-diisopropylamine; In methanol; 1,2-dichloro-ethane; isopropyl alcohol; toluene; acetonitrile; 1: Meerwein-Ponndorf-Verley reduction;
DOI:10.1016/j.bmcl.2011.12.008

Reference yield:

: C₁₇H₂₀ClNO₄

: 1360460-74-7
3β-benzoyloxy-8-(2-(3,5-dihydroxyphenyl)-2-oxoethyl)-8-azabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 2 steps

1: methanol / 22 h / 20 °C / Reflux

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 °C

With N-ethyl-N,N-diisopropylamine; In methanol; acetonitrile;
DOI:10.1016/j.bmcl.2011.12.008

Reference yield:

: 51863-60-6
3,5-dihydroxyacetophenone

: 1360460-74-7
3β-benzoyloxy-8-(2-(3,5-dihydroxyphenyl)-2-oxoethyl)-8-azabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 2 steps

1: copper(ll) bromide / dichloromethane; chloroform; ethyl acetate / 2 h / Reflux

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 °C

With N-ethyl-N,N-diisopropylamine; copper(ll) bromide; In dichloromethane; chloroform; ethyl acetate; acetonitrile;
DOI:10.1016/j.bmcl.2011.12.008