(1R,2S,3R,4S)-3-((E)-(2-hydroxy-3-methylbenzylidene)amino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Base Information

Chemical Name:(1R,2S,3R,4S)-3-((E)-(2-hydroxy-3-methylbenzylidene)amino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
CAS No.:1360459-99-9
Molecular Formula:C₁₈H₂₅NO₂
Molecular Weight:287.402
Hs Code.:

Synonyms:(1R,2S,3R,4S)-3-((E)-(2-hydroxy-3-methylbenzylidene)amino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

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Chemical Property of (1R,2S,3R,4S)-3-((E)-(2-hydroxy-3-methylbenzylidene)amino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

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Technology Process of (1R,2S,3R,4S)-3-((E)-(2-hydroxy-3-methylbenzylidene)amino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

There total 4 articles about (1R,2S,3R,4S)-3-((E)-(2-hydroxy-3-methylbenzylidene)amino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol 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: 86.0%

: 824-42-0
2-methoxy-3-methylbenzaldehyde

: 41719-73-7
(2S)-3-exo-aminoisoborneol

: 1360459-99-9
(1R,2S,3R,4S)-3-((E)-(2-hydroxy-3-methylbenzylidene)amino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Guidance literature:: With magnesium sulfate; triethylamine; In methanol; at 20 ℃; for 72h; Inert atmosphere;
DOI:10.1016/j.tetasy.2014.03.001

Reference yield:

: 736109-58-3,787517-91-3,68546-28-1
1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one

: 1360459-99-9
(1R,2S,3R,4S)-3-((E)-(2-hydroxy-3-methylbenzylidene)amino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium tert-butylate / 0 °C

1.2: 18 h / 0 °C

2.1: water / 16 h / Reflux

3.1: lithium aluminium tetrahydride / 24.8 h / 0 °C / Reflux

3.2: 20 °C

4.1: magnesium sulfate; triethylamine / methanol / 72 h / 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; potassium tert-butylate; water; magnesium sulfate; triethylamine; In methanol;
DOI:10.1016/j.tetasy.2014.03.001

Reference yield:

: 663-17-2
camphorquinone monooxime

: 1360459-99-9
(1R,2S,3R,4S)-3-((E)-(2-hydroxy-3-methylbenzylidene)amino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1.1: water / 16 h / Reflux

2.1: lithium aluminium tetrahydride / 24.8 h / 0 °C / Reflux

2.2: 20 °C

3.1: magnesium sulfate; triethylamine / methanol / 72 h / 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; water; magnesium sulfate; triethylamine; In methanol;
DOI:10.1016/j.tetasy.2014.03.001