(1R,2R,3R,5R)-3-[(1S)-α-methylbenzylamino]-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol

Base Information

Chemical Name:(1R,2R,3R,5R)-3-[(1S)-α-methylbenzylamino]-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol
CAS No.:1289376-23-3
Molecular Formula:C₁₈H₂₇NO
Molecular Weight:273.418
Hs Code.:

Synonyms:(1R,2R,3R,5R)-3-[(1S)-α-methylbenzylamino]-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol

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Chemical Property of (1R,2R,3R,5R)-3-[(1S)-α-methylbenzylamino]-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol

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Technology Process of (1R,2R,3R,5R)-3-[(1S)-α-methylbenzylamino]-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol

There total 3 articles about (1R,2R,3R,5R)-3-[(1S)-α-methylbenzylamino]-2,6,6-trimethylbicyclo[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: 95.0%

: 126003-98-3,126004-01-1,130714-54-4
(1R,2R,5R)-3-[(1S)-α-methylbenzylimino]-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol

: 1289376-23-3
(1R,2R,3R,5R)-3-[(1S)-α-methylbenzylamino]-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol

Guidance literature:: With sodium tris(acetoxy)borohydride; In isopropyl alcohol; at 20 ℃; for 6h; diastereoselective reaction; Inert atmosphere;
DOI:10.1007/s10600-011-9783-x

Reference yield:

: 7785-26-4,25766-18-1
(-)-α-pinene

: 1289376-23-3
(1R,2R,3R,5R)-3-[(1S)-α-methylbenzylamino]-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1: potassium permanganate

2: boron trifluoride diethyl etherate / benzene / 21 h / Reflux; Molecular sieve

3: sodium tris(acetoxy)borohydride / isopropyl alcohol / 6 h / 20 °C / Inert atmosphere

With potassium permanganate; boron trifluoride diethyl etherate; sodium tris(acetoxy)borohydride; In isopropyl alcohol; benzene;
DOI:10.1007/s10600-011-9783-x

Reference yield:

: 1845-25-6,10136-65-9,20536-50-9,73466-08-7,84236-04-4,125073-44-1,24047-72-1
(-)-(2R,3R,5R)-2-hydroxy-3-pinanone

: 1289376-23-3
(1R,2R,3R,5R)-3-[(1S)-α-methylbenzylamino]-2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: boron trifluoride diethyl etherate / benzene / 21 h / Reflux; Molecular sieve

2: sodium tris(acetoxy)borohydride / isopropyl alcohol / 6 h / 20 °C / Inert atmosphere

With boron trifluoride diethyl etherate; sodium tris(acetoxy)borohydride; In isopropyl alcohol; benzene;
DOI:10.1007/s10600-011-9783-x