(1R,2R,4R)-1-(diphenylaminomethyl)-7,7-dimethylbicyclo[2.2.1]hept-2-yl (E)-3-(pyrrolidin-1-yl)pent-2-enoate

Base Information

Chemical Name:(1R,2R,4R)-1-(diphenylaminomethyl)-7,7-dimethylbicyclo[2.2.1]hept-2-yl (E)-3-(pyrrolidin-1-yl)pent-2-enoate
CAS No.:1268671-95-9
Molecular Formula:C₃₁H₄₀N₂O₂
Molecular Weight:472.671
Hs Code.:

Synonyms:(1R,2R,4R)-1-(diphenylaminomethyl)-7,7-dimethylbicyclo[2.2.1]hept-2-yl (E)-3-(pyrrolidin-1-yl)pent-2-enoate

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Chemical Property of (1R,2R,4R)-1-(diphenylaminomethyl)-7,7-dimethylbicyclo[2.2.1]hept-2-yl (E)-3-(pyrrolidin-1-yl)pent-2-enoate

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Technology Process of (1R,2R,4R)-1-(diphenylaminomethyl)-7,7-dimethylbicyclo[2.2.1]hept-2-yl (E)-3-(pyrrolidin-1-yl)pent-2-enoate

There total 1 articles about (1R,2R,4R)-1-(diphenylaminomethyl)-7,7-dimethylbicyclo[2.2.1]hept-2-yl (E)-3-(pyrrolidin-1-yl)pent-2-enoate 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: 91.0%

: 123-75-1
pyrrolidine

: 1268671-81-3
(1R,2R,4R)-1-(diphenylaminomethyl)-7,7-dimethylbicyclo[2.2.1]hept-2-yl 3-oxopentanoate

: 1268671-95-9
(1R,2R,4R)-1-(diphenylaminomethyl)-7,7-dimethylbicyclo[2.2.1]hept-2-yl (E)-3-(pyrrolidin-1-yl)pent-2-enoate

Guidance literature:: With tert-butyl alcohol; In benzene; for 10h; Reflux;
DOI:10.1016/j.tet.2010.12.009

Reference yield:

: 1268671-95-9
(1R,2R,4R)-1-(diphenylaminomethyl)-7,7-dimethylbicyclo[2.2.1]hept-2-yl (E)-3-(pyrrolidin-1-yl)pent-2-enoate

: 616207-71-7,518348-13-5
(3S,4R,5S)-prelactone B

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 1.17 h / -78 - 20 °C

1.2: 2 h / -78 - 20 °C

2.1: hydrogenchloride; water / tetrahydrofuran / 22 h / 20 °C

3.1: 5% Pd(II)/C(eggshell); hydrogen / ethanol / 20 h / 760.05 Torr

With hydrogenchloride; 5% Pd(II)/C(eggshell); water; hydrogen; lithium diisopropyl amide; In tetrahydrofuran; ethanol;
DOI:10.1016/j.tet.2010.12.009