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(R)-2-[(tert-butoxycarbonyl)(methyl)amino]-1-phenylethanol

Base Information
  • Chemical Name:(R)-2-[(tert-butoxycarbonyl)(methyl)amino]-1-phenylethanol
  • CAS No.:291533-26-1
  • Molecular Formula:C14H21NO3
  • Molecular Weight:251.326
  • Hs Code.:
(R)-2-[(tert-butoxycarbonyl)(methyl)amino]-1-phenylethanol

Synonyms:(R)-2-[(tert-butoxycarbonyl)(methyl)amino]-1-phenylethanol

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Chemical Property of (R)-2-[(tert-butoxycarbonyl)(methyl)amino]-1-phenylethanol
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Technology Process of (R)-2-[(tert-butoxycarbonyl)(methyl)amino]-1-phenylethanol

There total 2 articles about (R)-2-[(tert-butoxycarbonyl)(methyl)amino]-1-phenylethanol 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 trans-RuCl2[(R)-xylbinap][(R)-daipen]; potassium tert-butylate; hydrogen; In isopropyl alcohol; tert-butyl alcohol; at 25 ℃; for 7h; under 6080.41 Torr;
DOI:10.1021/ja001098k
Guidance literature:
With potassium hydroxide; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; (1S,2R)-1-amino-2-indanol; In isopropyl alcohol; at 20 ℃; for 2h; Title compound not separated from byproducts;
DOI:10.1055/s-1999-2906
Guidance literature:
With hydrogenchloride; In diethyl ether; at 25 ℃; for 22h;
DOI:10.1021/ja001098k
upstream raw materials:

1,1-dimethylethyl methyl(2-phenyl-2-oxoethyl)carbamate

Downstream raw materials:

(-)-Halostachine

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