8-Azabicyclo[3.2.1]octane-3-methanol, (3-exo)-

Base Information

• Chemical Name: 8-Azabicyclo[3.2.1]octane-3-methanol, (3-exo)-
• CAS No.: 60941-77-7
• Molecular Formula: C8H15NO
• Molecular Weight: 141.213
• Hs Code.: 2902900000
• Mol file: 60941-77-7.mol

Synonyms:8-Azabicyclo[3.2.1]octane-3-methanol, (3-exo)-;(1R,5S)-8-azabicyclo[3.2.1]octan-3-ylMethanol;(1R,3s,5S)-8-Azabicyclo[3.2.1]octan-3-ylMethanol;exo-8-Azabicyclo[3.2.1]octane-3-Methanol

Chemical Property of 8-Azabicyclo[3.2.1]octane-3-methanol, (3-exo)-

Chemical Property:

• Boiling Point: 241.9±13.0 °C(Predicted)
• PKA: 14.93±0.10(Predicted)
• PSA: 32.26000
• Density: 1.026±0.06 g/cm3(Predicted)
• LogP: 0.83810
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C

Purity/Quality:

97% ^*data from raw suppliers

exo-8-Azabicyclo[3.2.1]octane-3-methanol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 8-Azabicyclo[3.2.1]octane-3-methanol, (3-exo)-

There total 5 articles about 8-Azabicyclo[3.2.1]octane-3-methanol, (3-exo)- 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:

(3-endo)-8-(phenylmethyl)-8-azabicyclo[3.2.1]oct-3-ylmethanol → 3β-Hydroxymethyl-nortropan (60941-77-7)

Guidance literature:

With hydrogenchloride; hydrogen; palladium hydroxide on carbon; In ethanol; water; at 20 ℃; for 48h; under 2844.39 Torr;

Reference yield:

tert-butyl 3-(hydroxymethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate (799283-62-8) → 8-azabicyclo[3.2.1]octan-3-ylmethanol (60941-77-7)

Guidance literature:

With hydrogenchloride; In dichloromethane; ethyl acetate; at 0 - 20 ℃; for 1h;

Reference yield:

tert-butyl 3-methylene-8-azabicyclo[3.2.1]octane-8-carboxylate (273207-57-1) → 8-azabicyclo[3.2.1]octan-3-ylmethanol (60941-77-7)

Guidance literature:

Multi-step reaction with 2 steps

1.1: borane-THF / tetrahydrofuran / 16 h / 0 - 15 °C

1.2: 2 h / 0 - 15 °C

2.1: hydrogenchloride / dichloromethane; ethyl acetate / 1 h / 0 - 20 °C

With hydrogenchloride; borane-THF; In tetrahydrofuran; dichloromethane; ethyl acetate;

upstream raw materials:

tert-butyl 3-methylene-8-azabicyclo[3.2.1]octane-8-carboxylate

tert-butyl 3-(hydroxymethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate

Downstream raw materials:

C₁₄H₁₉NO₄S

benzyl 3-(hydroxymethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate

[8-(4-morpholino-5-phenyl-thieno[2,3-d]pyrimidin-2-yl)-8-azabicyclo[3.2.1]octan-3-yl]methanol

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