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(2S,4R)-benzyl 2-(hydroxymethyl)-4-(1-methylcyclobutoxy)pyrrolidine-1-carboxylate

Base Information Edit
  • Chemical Name:(2S,4R)-benzyl 2-(hydroxymethyl)-4-(1-methylcyclobutoxy)pyrrolidine-1-carboxylate
  • CAS No.:1315591-69-5
  • Molecular Formula:C18H25NO4
  • Molecular Weight:319.401
  • Hs Code.:
  • Mol file:1315591-69-5.mol
(2S,4R)-benzyl 2-(hydroxymethyl)-4-(1-methylcyclobutoxy)pyrrolidine-1-carboxylate

Synonyms:(2S,4R)-benzyl 2-(hydroxymethyl)-4-(1-methylcyclobutoxy)pyrrolidine-1-carboxylate

Suppliers and Price of (2S,4R)-benzyl 2-(hydroxymethyl)-4-(1-methylcyclobutoxy)pyrrolidine-1-carboxylate
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Chemical Property of (2S,4R)-benzyl 2-(hydroxymethyl)-4-(1-methylcyclobutoxy)pyrrolidine-1-carboxylate Edit
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Technology Process of (2S,4R)-benzyl 2-(hydroxymethyl)-4-(1-methylcyclobutoxy)pyrrolidine-1-carboxylate

There total 4 articles about (2S,4R)-benzyl 2-(hydroxymethyl)-4-(1-methylcyclobutoxy)pyrrolidine-1-carboxylate 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:
(2S,4R)-benzyl 2-((tert-butyldiphenylsilyloxy)methyl)-4-(1-methylcyclobutoxy)pyrrolidine-1-carboxylate; With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 60h;
With water; In tetrahydrofuran; ethyl acetate;
Guidance literature:
Multi-step reaction with 4 steps
1: lithium borohydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere
2: 1H-imidazole / N,N-dimethyl-formamide / 20 °C / Inert atmosphere
3: boron trifluoride diethyl etherate / dichloromethane / 20 °C / Inert atmosphere; Sealed tube
4: tetrabutyl ammonium fluoride / tetrahydrofuran / 60 h / 20 °C
With 1H-imidazole; lithium borohydride; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 3 steps
1: 1H-imidazole / N,N-dimethyl-formamide / 20 °C / Inert atmosphere
2: boron trifluoride diethyl etherate / dichloromethane / 20 °C / Inert atmosphere; Sealed tube
3: tetrabutyl ammonium fluoride / tetrahydrofuran / 60 h / 20 °C
With 1H-imidazole; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
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