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(3R,5R)-1-benzyl-5-fluoropiperidin-3-amine

Base Information
  • Chemical Name:(3R,5R)-1-benzyl-5-fluoropiperidin-3-amine
  • CAS No.:1318129-36-0
  • Molecular Formula:C12H17FN2
  • Molecular Weight:208.279
  • Hs Code.:
(3R,5R)-1-benzyl-5-fluoropiperidin-3-amine

Synonyms:(3R,5R)-1-benzyl-5-fluoropiperidin-3-amine

Suppliers and Price of (3R,5R)-1-benzyl-5-fluoropiperidin-3-amine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 1 raw suppliers
Chemical Property of (3R,5R)-1-benzyl-5-fluoropiperidin-3-amine
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
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Technology Process of (3R,5R)-1-benzyl-5-fluoropiperidin-3-amine

There total 8 articles about (3R,5R)-1-benzyl-5-fluoropiperidin-3-amine 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:
Guidance literature:
With water; triphenylphosphine; In tetrahydrofuran; for 5h; chemoselective reaction; Inert atmosphere; Reflux;
DOI:10.1002/ejoc.201101829
Guidance literature:
((2S,4R)-1-benzyl-4-fluoropyrrolidin-2-yl)methanol; With tetrabutylammoniun azide; ethanaminium,N-(difluoro-λ4-sulfanylidene)-N-ethyl-,tetrafluoroborate; In dichloromethane; at -78 ℃; for 4h;
With water; triphenylphosphine; In tetrahydrofuran; for 5h; Reflux;
DOI:10.1021/ol201769b
Guidance literature:
Multi-step reaction with 3 steps
1.1: diethylamino-sulfur trifluoride / dichloromethane / 2.5 h / -78 - 20 °C
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / 0 °C
2.2: 0 °C
3.1: tetrabutylammoniun azide; ethanaminium,N-(difluoro-λ4-sulfanylidene)-N-ethyl-,tetrafluoroborate / dichloromethane / 4 h / -78 °C
3.2: 5 h / Reflux
With lithium aluminium tetrahydride; diethylamino-sulfur trifluoride; tetrabutylammoniun azide; ethanaminium,N-(difluoro-λ4-sulfanylidene)-N-ethyl-,tetrafluoroborate; In tetrahydrofuran; dichloromethane; 3.2: Staudinger reaction;
DOI:10.1021/ol201769b
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