(1R,2R,3S,5R)-3-benzylamino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-2-ol

Base Information

Chemical Name:(1R,2R,3S,5R)-3-benzylamino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-2-ol
CAS No.:1370261-56-5
Molecular Formula:C₁₇H₂₅NO₂
Molecular Weight:275.391
Hs Code.:

Synonyms:(1R,2R,3S,5R)-3-benzylamino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-2-ol

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Chemical Property of (1R,2R,3S,5R)-3-benzylamino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-2-ol

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Technology Process of (1R,2R,3S,5R)-3-benzylamino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-2-ol

There total 3 articles about (1R,2R,3S,5R)-3-benzylamino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]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:

: 1370261-51-0
2,2,2-trichloro-N-((1R,2R,3S,5R)-2-hydroxy-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-3-yl)acetamide

: 1370261-56-5
(1R,2R,3S,5R)-3-benzylamino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogenchloride / diethyl ether; water / 24 h / 20 °C

2.1: triethylamine / ethanol / 2 h / 20 °C

2.2: 24 h / 20 °C

With hydrogenchloride; triethylamine; In diethyl ether; ethanol; water;
DOI:10.1016/j.tetasy.2012.01.020

Reference yield:

: 199801-80-4
2,2,2-trichloro-N-((1R,3S,5R)-6,6-dimethyl-2-methylenebicyclo[3.1.1]heptan-3-yl)acetamide

: 1370261-56-5
(1R,2R,3S,5R)-3-benzylamino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / water; acetone; tert-butyl alcohol / 24 h / 20 °C

2.1: hydrogenchloride / diethyl ether; water / 24 h / 20 °C

3.1: triethylamine / ethanol / 2 h / 20 °C

3.2: 24 h / 20 °C

With hydrogenchloride; osmium(VIII) oxide; 4-methylmorpholine N-oxide; triethylamine; In diethyl ether; ethanol; water; acetone; tert-butyl alcohol;
DOI:10.1016/j.tetasy.2012.01.020

Reference yield:

: 19894-97-4
(1R)-Myrtenol

: 1370261-56-5
(1R,2R,3S,5R)-3-benzylamino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 0 °C

1.2: 24 h / Reflux

2.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / water; acetone; tert-butyl alcohol / 24 h / 20 °C

3.1: hydrogenchloride / diethyl ether; water / 24 h / 20 °C

4.1: triethylamine / ethanol / 2 h / 20 °C

4.2: 24 h / 20 °C

With hydrogenchloride; osmium(VIII) oxide; 4-methylmorpholine N-oxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In diethyl ether; ethanol; dichloromethane; water; acetone; tert-butyl alcohol; 1.2: Overman rearrangement;
DOI:10.1016/j.tetasy.2012.01.020